@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_head {
  this: np:hasAssertion dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_assertion;
    np:hasProvenance dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_provenance;
    np:hasPublicationInfo dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_assertion a np:Assertion .
  
  dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_provenance a np:Provenance .
  
  dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0032460 a ncit:C7057 .
  
  dgn-gda:DGN89d21fff3219e03864d2cd136c43b2be sio:SIO_000628 miriam-gene:367, lld:C0032460;
    a sio:SIO_001122 .
}

dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_provenance {
  dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_assertion dcterms:description
      "[Association of shorter CAG repeats with PCOS is consistent with in vitro functional studies demonstrating higher activity of androgen receptors expressed from alleles with fewer CAG repeats, suggesting inherited alteration in androgen sensitivity may contribute to PCOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:18303071;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP85963.RA146yvfjxVZJv2h1wsk27UXCiNnEBZ-wlxzlMfh-wQa0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}