@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA> .
@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:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_head {
  this: np:hasAssertion dgn-np:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_assertion;
    np:hasProvenance dgn-np:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_provenance;
    np:hasPublicationInfo dgn-np:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_assertion a np:Assertion .
  
  dgn-np:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_provenance a np:Provenance .
  
  dgn-np:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0014130 a ncit:C7057 .
  
  dgn-gda:DGNf74db2694f4e2135ebc10a927e5d9aad sio:SIO_000628 miriam-gene:1312, lld:C0014130;
    a sio:SIO_001122 .
}

dgn-np:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_provenance {
  dgn-np:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_assertion dcterms:description
      "[ Genetic variation in CYP19 and SHBG contributes to variance in circulating hormone levels between postmenopausal women, but low r2 values may explain why these genes have given inconclusive results in breast cancer case-control studies.]. 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:15199113;
    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:NP59920.RAd_sm73yxeA9Dhjzth383QLNdwcD992wQ-xWIAgYTdzA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}