@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4> .
@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:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_head {
  this: np:hasAssertion dgn-np:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_assertion;
    np:hasProvenance dgn-np:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_provenance;
    np:hasPublicationInfo dgn-np:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_assertion a np:Assertion .
  
  dgn-np:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_provenance a np:Provenance .
  
  dgn-np:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_assertion {
  miriam-gene:3643 a ncit:C16612 .
  
  lld:C0032460 a ncit:C7057 .
  
  dgn-gda:DGN0da5cba74c2a8c4caf6df91d4094eaad sio:SIO_000628 miriam-gene:3643, lld:C0032460;
    a sio:SIO_001122 .
}

dgn-np:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_provenance {
  dgn-np:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_assertion dcterms:description
      "[In conclusion, our results suggested that a susceptibility gene for PCOS was located on chromosome 19p13.3 in the insulin receptor gene region. It remains to be determined if this susceptibility gene is the insulin receptor gene itself or a closely located gene. Since insulin stimulates androgen secretion by the ovarian stroma it is likely that INSR function in the ovary is involved in the genetic susceptibility ot 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:11232039;
    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:NP55863.RAdXX_lDQN_OU3gyC3OCQz8uVa-JWatN_cbJtTXcGYAn4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}