@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU> .
@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:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_head {
  this: np:hasAssertion dgn-np:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_assertion;
    np:hasProvenance dgn-np:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_provenance;
    np:hasPublicationInfo dgn-np:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_assertion a np:Assertion .
  
  dgn-np:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_provenance a np:Provenance .
  
  dgn-np:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0032460 a ncit:C7057 .
  
  dgn-gda:DGN4abbb50e6122eb58752d7ee50e161631 sio:SIO_000628 miriam-gene:367, lld:C0032460;
    a sio:SIO_001121 .
}

dgn-np:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_provenance {
  dgn-np:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_assertion dcterms:description
      "[The present study was carried out to assess the role of androgen receptor CAG repeat polymorphism and X chromosome inactivation (XCI) pattern among Indian PCOS women and controls which has not been hitherto explored and also to test the hypothesis that shorter CAG alleles would be preferentially activated in 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:20865044;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP490850.RA4l0HeuQJbYFY9G4Why919oUXzYBsTVJqGrS2vtWAYmU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:53+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" .
}