UNKNOWN
type: MediaType
mimetype: UNKNOWN

ApplicationJson
type: MediaType
mimetype: application/json

TextPlain
type: MediaType
mimetype: text/plain

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: orig
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=orig.owl
format extension: owl
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: <?xml version="1.0"?> <rdf:RDF xmlns="https://w3id.org/hereditary/ontology/phenoclinical/schema/" xml:base="https://w3id.org/hereditary/ontology/phenoclinical/schema/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:ns="http://creativecommons.org/ns#" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:xml="http://www.w3.org/XML/1998/namespace" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" xmlns:adms="http://www.w3.org/ns/adms#"
type: orig
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:29Z
publisher: onto
byte size: 929301
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=orig.owl
media type: ApplicationRDFXML

TextTurtle
type: MediaType
mimetype: text/turtle

The Hereditary Ontology for Phenoclinical Data
type: Dataset
comment: The Hereditary ontology models clinical and genomics data to provide a unifying layer to query different database sources through an Ontology-Based Data Access (OBDA) framework.
account: ontologies
artifact: hereditary--ontology--phenoclinical--schema
associated agent: onto
group: w3id.org
groupdocu: ## All DBpedia Archivo ontologies from w3id.org domain Each artifact in this group deals as the archive for snapshots of one ontology of the [DBpedia Archivo](https://databus.dbpedia.org/ontologies) - A Web-Scale Interface for Ontology Archiving under Consumer-oriented Aspects. Find out more at [http://archivo.dbpedia.org](http://archivo.dbpedia.org). The description for the individual files in the artifact can be found [here](http://dev.dbpedia.org/DBpedia_Archvio#files).
maintainer: onto
version: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415
conforms to: http://dataid.dbpedia.org/ns/core#
description: ## DBpedia Archivo Ontology Snapshot | Attribute | Value | | - | - | | Ontology URI | <https://w3id.org/hereditary/ontology/phenoclinical/schema/> | Archivo Ontology Factsheet| [Link](http://archivo.dbpedia.org/info?o=https://w3id.org/hereditary/ontology/phenoclinical/schema/) | Snapshot File URL | <https://hereditary.dei.unipd.it/ontology/phenoclinical/schema/hero_phenoclinical.owl> | Snapshot OWL Version IRI | <https://w3id.org/hereditary/ontology/phenoclinical/1.0/> | Snapshot Time | 2024-11-24 07:44:15 The [DBpedia Archivo Databus agent](https://databus.dbpedia.org/ontologies) generates only basic, static documentation for the archived snapshots of the ontologies. ## Ontology Metadata DBpedia Archivo extracts metadata from the ontology for well known properties (e.g. dct:description). This subsection shows the content of every property individually using a separate heading. ### dct:description The Hereditary ontology models clinical and genomics data to provide a unifying layer to query different database sources through an Ontology-Based Data Access (OBDA) framework. This part of the ontology focuses on phenoclinical data for ALS and MS patients. ### rdfs:comment A functional unit of heredity which occupies a specific position on a particular chromosome and serves as the template for a product that contributes to a phenotype or a biological function. [Definition Source: NCIT] The taxonomy is based on NCIT. ### rdfs:comment This taxonomy describes the type of surgical procedures. The taxonomy is based on SNOMED-CT. ### rdfs:comment This taxonomy comprises disease, disorder or findings. The taxonomy is mainly based on NCIT. ### rdfs:comment Any detrimental or unintended response associated with the use of a medication in humans. [Definition Source: NCIT] The taxonomy is based on OAE. ### rdfs:comment This taxonomy describes the different type of relative a person can have. The taxonomy is based on NCIT. ### rdfs:comment This taxonomy describes the occupation of a…
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
publisher: onto
distribution: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: pelletConsistency
content variant: FULL
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=pelletConsistency_imports=FULL.txt
format extension: txt
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: There are 1 input files: /usr/local/archivo-data/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=parsed.ttl Start loading Nov 24, 2024 7:44:43 AM org.mindswap.pellet.jena.graph.loader.DefaultGraphLoader addUnsupportedFeature WARNING: Unsupported axiom: Ignoring triple with unknown property from OWL namespace: https://w3id.org/hereditary/ontology/phenoclinical/schema/ @owl:versionIRI https://w3id.org/hereditary/ontology/phenoclinical/1.0/ Finished loading in 00:00:00.664 Input size: Classes = 97, Properties = 319, Individuals = 713 Expressivity: ALCHF(D) Start consistency check Finished consistency check in 00:00:00.090
imports: FULL
type: pelletConsistency
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:46Z
publisher: onto
byte size: 890
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=pelletConsistenc…
media type: TextPlain

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: meta
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=meta.json
format extension: json
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: { "http-data": { "accessed": "2024.11.24; 07:44:29", "best-header": "application/rdf+xml", "content-length": "929300", "e-tag": "\"e2e14-626670935ecba\"", "lastModified": "Fri, 08 Nov 2024 13:50:38 GMT" }, "logs": { "nir-header": "{'Date': 'Sun, 24 Nov 2024 07:44:19 GMT', 'Server': 'Apache/2.4.29 (Ubuntu)', 'Access-Control-Allow-Origin': '*', 'Location': 'http://hereditary.dei.unipd.it/ontology/phenoclinical/schema/hero_phenoclinical.owl', 'Content-Length': '365', 'Keep-Alive': 'timeout=5, max=100', 'Connection': 'Keep-Alive', 'Content-Type': 'text/html; charset=iso-8859-1'}",
type: meta
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:45:01Z
publisher: onto
byte size: 1527
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=meta.json
media type: ApplicationJson

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: pelletInfo
content variant: NONE
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=pelletInfo_imports=NONE.txt
format extension: txt
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: WARNING: An illegal reflective access operation has occurred WARNING: Illegal reflective access by com.google.inject.internal.cglib.core.$ReflectUtils$2 (file:/usr/lib/pellet/cli/target/pelletcli/lib/guice-4.0.jar) to method java.lang.ClassLoader.defineClass(java.lang.String,byte[],int,int,java.security.ProtectionDomain) WARNING: Please consider reporting this to the maintainers of com.google.inject.internal.cglib.core.$ReflectUtils$2 WARNING: Use --illegal-access=warn to enable warnings of further illegal reflective access operations WARNING: All illegal access operations will be denied in a future release [main] WARN org.semanticweb.owlapi.util.SAXParsers - http://www.oracle.com/xml/jaxp/properties/entityExpansionLimit not supported by parser type org.apache.xerces.jaxp.SAXParserImpl [main] WARN org.semanticweb.owlapi.util.SAXParsers - entityExpansionLimit not supported by parser type org.apache.xerces.jaxp.SAXParserImpl [main] WARN org.semanticweb.owlapi.util.SAXParsers - http://www.oracle.com/xml/jaxp/properties/entityExpansionLimit not supported by parser type org.apache.xerces.jaxp.SAXParserImpl [main] WARN org.semanticweb.owlapi.util.SAXParsers - entityExpansionLimit not supported by parser type org.apache.xerces.jaxp.SAXParserImpl [main] WARN org.semanticweb.owlapi.util.SAXParsers - http://www.oracle.com/xml/jaxp/properties/entityExpansionLimit not supported by parser type org.apache.xerces.jaxp.SAXParserImpl
imports: NONE
type: pelletInfo
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:55Z
publisher: onto
byte size: 12387
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=pelletInfo_impor…
media type: TextPlain

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: diff
content variant: new
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=diff_axioms=new.dl
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
axioms: new
type: diff
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:37Z
publisher: onto
byte size: 1
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=diff_axioms=new.…
media type: UNKNOWN

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: parsed
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=parsed.ttl
format extension: ttl
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: @prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> . @prefix : <https://w3id.org/hereditary/ontology/phenoclinical/schema/> . @prefix dc: <http://purl.org/dc/elements/1.1/> . @prefix ns: <http://creativecommons.org/ns#> . @prefix owl: <http://www.w3.org/2002/07/owl#> . @prefix xml: <http://www.w3.org/XML/1998/namespace> . @prefix xsd: <http://www.w3.org/2001/XMLSchema#> . @prefix adms: <http://www.w3.org/ns/adms#> . @prefix foaf: <http://xmlns.com/foaf/0.1/> . @prefix om-1: <http://www.wurvoc.org/vocabularies/om-1.8/> .
type: parsed
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:37Z
publisher: onto
byte size: 570075
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=parsed.ttl
media type: TextTurtle

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: old
content variant: diff
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=diff_triples=old.nt
format extension: nt
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://purl.org/dc/terms/license> "Copyright 2024-2027 University of Padua, Italy\n\nLicensed under the\n\nCreative Commons Attribution 4.0 International License\n https://creativecommons.org/licenses/by/4.0/\n\nYou may obtain a copy of the License at\n https://creativecommons.org/licenses/by/4.0/legalcode\n\nThis work has been supported by the HEREDITARY project\n https://hereditary-project.eu/\n\n funded by the European Union\u2019s Horizon Europe research and innovation programme \n under the grant agreement No GA101137074" . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://purl.org/dc/terms/title> "The Hereditary Ontology for Phenoclinical Data"@en . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://www.w3.org/2000/01/rdf-schema#comment> "The Hereditary ontology models clinical and genomics data to provide a unifying layer to query different database sources through an Ontology-Based Data Access (OBDA) framework. This part of the ontology focuses on phenoclinical data for ALS and MS patients."@en .
triples: old
type: diff
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:37Z
publisher: onto
byte size: 1139
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=diff_triples=old…
media type: ApplicationNTriples

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: diff
content variant: new
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=diff_triples=new.nt
format extension: nt
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://purl.org/dc/elements/1.1/title> "The Hereditary Ontology for Phenoclinical Data"@en . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://purl.org/dc/terms/description> "The Hereditary ontology models clinical and genomics data to provide a unifying layer to query different database sources through an Ontology-Based Data Access (OBDA) framework. This part of the ontology focuses on phenoclinical data for ALS and MS patients."@en . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://purl.org/dc/terms/license> "Copyright 2024-2027 University of Padua, Italy\n\nLicensed under the\n\nCreative Commons Attribution 4.0 International License\n https://creativecommons.org/licenses/by/4.0/\n\nYou may obtain a copy of the License at\n https://creativecommons.org/licenses/by/4.0/legalcode\n\nThis work has been supported by the HEREDITARY project\n https://hereditary-project.eu/\n\n funded by the European Union\u2019s Horizon Europe research and innovation programme \n under the grant agreement No GA101137074"@en .
triples: new
type: diff
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:37Z
publisher: onto
byte size: 1141
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=diff_triples=new…
media type: ApplicationNTriples

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: profile
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=profile.txt
format extension: txt
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: WARNING: An illegal reflective access operation has occurred WARNING: Illegal reflective access by com.google.inject.internal.cglib.core.$ReflectUtils$1 (file:/usr/local/src/webapp/archivo/archivo/helpingBinaries/profilechecker-1.1.0.jar) to method java.lang.ClassLoader.defineClass(java.lang.String,byte[],int,int,java.security.ProtectionDomain) WARNING: Please consider reporting this to the maintainers of com.google.inject.internal.cglib.core.$ReflectUtils$1 WARNING: Use --illegal-access=warn to enable warnings of further illegal reflective access operations WARNING: All illegal access operations will be denied in a future release [main] ERROR uk.ac.manchester.cs.owl.owlapi.OWLOntologyManagerImpl - Illegal redeclarations of entities: reuse of entity http://www.wurvoc.org/vocabularies/om-1.8/symbol in punning not allowed [Declaration(AnnotationProperty(<http://www.wurvoc.org/vocabularies/om-1.8/symbol>)), Declaration(DataProperty(<http://www.wurvoc.org/vocabularies/om-1.8/symbol>))] [main] INFO org.semanticweb.owlapi.rdf.rdfxml.parser.TripleHandlers - Usage of rdf vocabulary: http://www.w3.org/2004/02/skos/core#inScheme -> http://www.w3.org/1999/02/22-rdf-syntax-ns#type -> http://www.w3.org/1999/02/22-rdf-syntax-ns#Property [main] INFO org.semanticweb.owlapi.rdf.rdfxml.parser.TripleHandlers - Usage of rdf vocabulary: http://www.w3.org/2004/02/skos/core#hasTopConcept -> http://www.w3.org/1999/02/22-rdf-syntax-ns#type -> http://www.w3.org/1999/02/22-rdf-syntax-ns#Property [main] INFO org.semanticweb.owlapi.rdf.rdfxml.parser.TripleHandlers - Usage of rdf vocabulary: http://www.w3.org/2004/02/skos/core#topConceptOf -> http://www.w3.org/1999/02/22-rdf-syntax-ns#type -> http://www.w3.org/1999/02/22-rdf-syntax-ns#Property [main] INFO org.semanticweb.owlapi.rdf.rdfxml.parser.TripleHandlers - Usage of rdf vocabulary: http://www.w3.org/2004/02/skos/core#prefLabel -> http://www.w3.org/1999/02/22-rdf-syntax-ns#type -> http://www.w3.org/1999/02/22-rdf-syntax-ns#Property
type: profile
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:45:01Z
publisher: onto
byte size: 8430
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=profile.txt
media type: TextPlain

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: shaclReport
content variant: minLicense
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=shaclReport_validates=minLicense.ttl
format extension: ttl
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: @prefix sh: <http://www.w3.org/ns/shacl#> . @prefix xsd: <http://www.w3.org/2001/XMLSchema#> . [] a sh:ValidationReport ; sh:conforms false ; sh:result [ a sh:ValidationResult ; sh:focusNode <http://purl.obolibrary.org/obo/NCIT_C13717> ; sh:resultMessage "No license found at all (neither dct:license, xhv:license nor cc:license)"@en ; sh:resultSeverity sh:Violation ; sh:sourceConstraintComponent sh:OrConstraintComponent ;
type: shaclReport
validates: minLicense
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:39Z
publisher: onto
byte size: 5854
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=shaclReport_vali…
media type: ApplicationNTriples

ApplicationNTriples
type: MediaType
mimetype: application/n-triples

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: goodLicense
content variant: shaclReport
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=shaclReport_validates=goodLicense.ttl
format extension: ttl
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: @prefix dct: <http://purl.org/dc/terms/> . @prefix sh: <http://www.w3.org/ns/shacl#> . @prefix xsd: <http://www.w3.org/2001/XMLSchema#> . [] a sh:ValidationReport ; sh:conforms false ; sh:result [ a sh:ValidationResult ; sh:focusNode <https://w3id.org/hereditary/ontology/phenoclinical/schema/groupTaxonomy> ; sh:resultMessage "No dct:license statement found"@en ; sh:resultPath dct:license ;
type: shaclReport
validates: goodLicense
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:41Z
publisher: onto
byte size: 6063
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=shaclReport_vali…
media type: ApplicationNTriples

ApplicationRDFXML
type: MediaType
mimetype: application/rdf+xml

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: diff
content variant: old
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=diff_axioms=old.dl
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
axioms: old
type: diff
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:37Z
publisher: onto
byte size: 1
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=diff_axioms=old.…
media type: UNKNOWN

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: archivoMetadata
content variant: shaclReport
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=shaclReport_validates=archivoMetadata.ttl
format extension: ttl
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: @prefix sh: <http://www.w3.org/ns/shacl#> . @prefix xsd: <http://www.w3.org/2001/XMLSchema#> . [] a sh:ValidationReport ; sh:conforms false ; sh:result [ a sh:ValidationResult ; sh:focusNode <https://w3id.org/hereditary/ontology/phenoclinical/schema/kinshipTypeTaxonomy> ; sh:resultMessage "Archivo requires either dct:abstract, dct:description or dc:description for a short comment about the ontology."@en ; sh:resultSeverity sh:Violation ; sh:sourceConstraintComponent sh:OrConstraintComponent ;
type: shaclReport
validates: archivoMetadata
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:39Z
publisher: onto
byte size: 6374
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=shaclReport_vali…
media type: ApplicationNTriples

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: parsed
content variant: sorted
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=parsed_sorted.nt
format extension: nt
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: <http://creativecommons.org/ns#license> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.w3.org/2002/07/owl#AnnotationProperty> . <http://data.europa.eu/esco/isco/C01> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.w3.org/2002/07/owl#NamedIndividual> . <http://data.europa.eu/esco/isco/C01> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.w3.org/2004/02/skos/core#Concept> . <http://data.europa.eu/esco/isco/C01> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <https://w3id.org/brainteaser/ontology/schema/Occupation> . <http://data.europa.eu/esco/isco/C01> <http://www.w3.org/2000/01/rdf-schema#comment> "Commissioned armed forces officers provide leadership and management to organizational units in the armed forces and/or perform similar tasks to those performed in a variety of civilian occupations outside the armed forces. This group includes all members of the armed forces holding the rank of second lieutenant (or equivalent) or higher. Competent performance in most occupations in this sub-major group requires skills at the fourth ISCO skill level.\nOccupations in this sub-major group are classified into the following minor group:\n011 Commissioned Armed Forces Officers\nExcluded from this group are:\n- jobs held by persons in civilian employment of government establishments concerned with defence issues;\n- police (other than military police);\n- customs inspectors and members of border or other armed civilian services."@en . <http://data.europa.eu/esco/isco/C01> <http://www.w3.org/2000/01/rdf-schema#label> "Commissioned armed forces officers"@en . <http://data.europa.eu/esco/isco/C01> <http://www.w3.org/2004/02/skos/core#broaderTransitive> <http://data.europa.eu/esco/isco/C0> . <http://data.europa.eu/esco/isco/C01> <http://www.w3.org/2004/02/skos/core#inScheme> <https://w3id.org/hereditary/ontology/phenoclinical/schema/occupationTaxonomy> . <http://data.europa.eu/esco/isco/C02> <http://www.w3.org/1999/02/22-rdf-syntax-ns#ty…
tag: sorted
type: parsed
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:29Z
publisher: onto
byte size: 1267554
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=parsed_sorted.nt
media type: ApplicationNTriples

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: pelletInfo
content variant: FULL
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=pelletInfo_imports=FULL.txt
format extension: txt
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: WARNING: An illegal reflective access operation has occurred WARNING: Illegal reflective access by com.google.inject.internal.cglib.core.$ReflectUtils$2 (file:/usr/lib/pellet/cli/target/pelletcli/lib/guice-4.0.jar) to method java.lang.ClassLoader.defineClass(java.lang.String,byte[],int,int,java.security.ProtectionDomain) WARNING: Please consider reporting this to the maintainers of com.google.inject.internal.cglib.core.$ReflectUtils$2 WARNING: Use --illegal-access=warn to enable warnings of further illegal reflective access operations WARNING: All illegal access operations will be denied in a future release [main] WARN org.semanticweb.owlapi.util.SAXParsers - http://www.oracle.com/xml/jaxp/properties/entityExpansionLimit not supported by parser type org.apache.xerces.jaxp.SAXParserImpl [main] WARN org.semanticweb.owlapi.util.SAXParsers - entityExpansionLimit not supported by parser type org.apache.xerces.jaxp.SAXParserImpl [main] WARN org.semanticweb.owlapi.util.SAXParsers - http://www.oracle.com/xml/jaxp/properties/entityExpansionLimit not supported by parser type org.apache.xerces.jaxp.SAXParserImpl [main] WARN org.semanticweb.owlapi.util.SAXParsers - entityExpansionLimit not supported by parser type org.apache.xerces.jaxp.SAXParserImpl [main] WARN org.semanticweb.owlapi.util.SAXParsers - http://www.oracle.com/xml/jaxp/properties/entityExpansionLimit not supported by parser type org.apache.xerces.jaxp.SAXParserImpl
imports: FULL
type: pelletInfo
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:50Z
publisher: onto
byte size: 12387
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=pelletInfo_impor…
media type: TextPlain

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: lodeMetadata
content variant: shaclReport
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=shaclReport_validates=lodeMetadata.ttl
format extension: ttl
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: @prefix dc: <http://purl.org/dc/elements/1.1/> . @prefix owl: <http://www.w3.org/2002/07/owl#> . @prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> . @prefix sh: <http://www.w3.org/ns/shacl#> . @prefix xsd: <http://www.w3.org/2001/XMLSchema#> . [] a sh:ValidationReport ; sh:conforms false ; sh:result [ a sh:ValidationResult ; sh:focusNode <https://w3id.org/brainteaser/ontology/schema/alsfrs7> ;
type: shaclReport
validates: lodeMetadata
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:41Z
publisher: onto
byte size: 188368
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=shaclReport_vali…
media type: ApplicationNTriples

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: parsed
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=parsed.owl
format extension: owl
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: <?xml version="1.0" encoding="utf-8"?> <rdf:RDF xmlns:Pollution="http://ontology.eil.utoronto.ca/GCI/Environment/Pollution.owl#" xmlns:adms="http://www.w3.org/ns/adms#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:ns="http://creativecommons.org/ns#" xmlns:om-1="http://www.wurvoc.org/vocabularies/om-1.8/" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#" xmlns:skos="http://www.w3.org/2004/02/skos/core#" xmlns:terms="http://purl.org/dc/terms/" xmlns:vann="http://purl.org/vocab/vann/" xmlns:xml="http://www.w3.org/XML/1998/namespace" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" xmlns="https://w3id.org/hereditary/ontology/phenoclinical/schema/"> <rdf:Description rdf:about="https://w3id.org/hereditary/ontology/phenoclinical/schema/"> <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#Ontology"/> </rdf:Description> <rdf:Description rdf:about="https://w3id.org/hereditary/ontology/phenoclinical/schema/"> <owl:versionIRI rdf:resource="https://w3id.org/hereditary/ontology/phenoclinical/1.0/"/> </rdf:Description> <rdf:Description rdf:about="https://w3id.org/hereditary/ontology/phenoclinical/schema/"> <owl:imports rdf:resource="http://ontology.eil.utoronto.ca/GCI/Environment/Pollution.owl"/>
type: parsed
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:38Z
publisher: onto
byte size: 1539678
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=parsed.owl
media type: ApplicationRDFXML

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: pelletConsistency
content variant: NONE
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=pelletConsistency_imports=NONE.txt
format extension: txt
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: There are 1 input files: /usr/local/archivo-data/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=parsed.ttl Start loading Nov 24, 2024 7:44:45 AM org.mindswap.pellet.jena.graph.loader.DefaultGraphLoader addUnsupportedFeature WARNING: Unsupported axiom: Ignoring triple with unknown property from OWL namespace: https://w3id.org/hereditary/ontology/phenoclinical/schema/ @owl:versionIRI https://w3id.org/hereditary/ontology/phenoclinical/1.0/ Finished loading in 00:00:00.614 Input size: Classes = 97, Properties = 319, Individuals = 713 Expressivity: ALCHF(D) Start consistency check Finished consistency check in 00:00:00.072
imports: NONE
type: pelletConsistency
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:46Z
publisher: onto
byte size: 890
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=pelletConsistenc…
media type: TextPlain

https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/dataid.ttl
type: SingleFile
associated agent: onto
compression: None
content variant: parsed
file: https://databus.dbpedia.org/ontologies/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=parsed.nt
format extension: nt
is distribution of: The Hereditary Ontology for Phenoclinical Data
maintainer: onto
preview: <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.w3.org/2002/07/owl#Ontology> . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://www.w3.org/2002/07/owl#versionIRI> <https://w3id.org/hereditary/ontology/phenoclinical/1.0/> . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://www.w3.org/2002/07/owl#imports> <http://ontology.eil.utoronto.ca/GCI/Environment/Pollution.owl> . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://www.w3.org/2002/07/owl#imports> <http://www.w3.org/2004/02/skos/core> . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://purl.org/dc/elements/1.1/title> "The Hereditary Ontology for Phenoclinical Data"@en . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://purl.org/dc/terms/creator> <https://orcid.org/0000-0002-0676-682X> . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://purl.org/dc/terms/creator> <https://orcid.org/0000-0003-4970-4554> . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://purl.org/dc/terms/description> "The Hereditary ontology models clinical and genomics data to provide a unifying layer to query different database sources through an Ontology-Based Data Access (OBDA) framework. This part of the ontology focuses on phenoclinical data for ALS and MS patients."@en . <https://w3id.org/hereditary/ontology/phenoclinical/schema/> <http://purl.org/dc/terms/license> "Copyright 2024-2027 University of Padua, Italy\n\nLicensed under the\n\nCreative Commons Attribution 4.0 International License\n https://creativecommons.org/licenses/by/4.0/\n\nYou may obtain a copy of the License at\n https://creativecommons.org/licenses/by/4.0/legalcode\n\nThis work has been supported by the HEREDITARY project\n https://hereditary-project.eu/\n\n funded by the European Union\u2019s Horizon Europe research and innovation programme \n under the grant agreemen…
type: parsed
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 2024.11.24-074415
issued: 2024-11-24T07:45:18Z
license: notAnIRI
modified: 2024-11-24T07:44:37Z
publisher: onto
byte size: 1267554
download URL: https://akswnc7.informatik.uni-leipzig.de/dstreitmatter/archivo/w3id.org/hereditary--ontology--phenoclinical--schema/2024.11.24-074415/hereditary--ontology--phenoclinical--schema_type=parsed.nt
media type: ApplicationNTriples

DataID metadata for w3id.org/hereditary--ontology--phenoclinical--schema
type: DataId
comment: Metadata created by the DBpedia Databus Maven Plugin: https://github.com/dbpedia/databus-maven-plugin (Version 1.3-SNAPSHOT) The DataID ontology is a metadata omnibus, which can be extended to be interoperable with all metadata formats Note that the metadata (the dataid.ttl file) is always CC-0, the files are licensed individually Metadata created by https://yum-yab.github.io/webid.ttl#onto
associated agent: onto
conforms to: http://dataid.dbpedia.org/ns/core#
has version: 1.3-SNAPSHOT
issued: 2024-11-24T07:45:18Z
license: cc-zero1.0
publisher: onto