@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw> .
@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:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_head {
  this: np:hasAssertion dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_assertion;
    np:hasProvenance dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_provenance;
    np:hasPublicationInfo dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_assertion a np:Assertion .
  
  dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_provenance a np:Provenance .
  
  dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_assertion {
  miriam-gene:1586 a ncit:C16612 .
  
  lld:C3277849 a ncit:C7057 .
  
  dgn-gda:DGNbfc397a8c78bf92f697aafe32be3967a sio:SIO_000628 miriam-gene:1586, lld:C3277849;
    a sio:SIO_001121 .
}

dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_provenance {
  dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_assertion dcterms:description
      "[Isolated 17,20 lyase deficiency is rare, but the identification of its genetic basis and the study of P450c17 enzymology have recently clarified the mechanisms by which DHEA synthesis may be regulated in adrenarche, and have suggested that the lesion underlying polycystic ovary syndrome might involve a serine kinase.]. 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:9890062;
    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:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:29+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" .
}