@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo> .
@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:NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo130_head {
  this: np:hasAssertion dgn-np:NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo130_assertion ;
    np:hasProvenance dgn-np:NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo130_provenance ;
    np:hasPublicationInfo dgn-np:NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo130_provenance a np:Provenance .
  dgn-np:NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo130_assertion {
  miriam-gene:1586 a ncit:C16612 .
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}
dgn-np:NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo130_provenance {
  dgn-np:NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo130_assertion dcterms:description "[We designed the present study in order to evaluate the eventual role of polymorphisms in the genes encoding cytochrome P450c17alpha (CYP17) and the progesterone receptor (PROGINS) as risk factors for endometriosis development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    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:NP404047.RAC_2s76EUe3zj9bu698czX_rFazo9khyb-HdTCMCCCuo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:00+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}