@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes> .
@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:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_head {
  this: np:hasAssertion dgn-np:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_assertion;
    np:hasProvenance dgn-np:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_provenance;
    np:hasPublicationInfo dgn-np:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_assertion a np:Assertion .
  
  dgn-np:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_provenance a np:Provenance .
  
  dgn-np:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  
  lld:C0235461 a ncit:C7057 .
  
  dgn-gda:DGN8bd412f687bd346a4317b5093c230e66 sio:SIO_000628 miriam-gene:3630, lld:C0235461;
    a sio:SIO_001121 .
}

dgn-np:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_provenance {
  dgn-np:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_assertion dcterms:description
      "[It is suggested that, in human females, exposure to excess androgen, at any stage from fetal development of the ovary to the onset of puberty, leads to many of the characteristic features of PCOS, including abnormalities of luteinizing hormone secretion and insulin resistance.]. 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:16390494;
    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:NP679560.RAtf73Qi8pHuKcGz9fV_K_S57SWFtMaBDrZkZrY6MLaes130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:50+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" .
}