@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ> .
@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:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_head {
  this: np:hasAssertion dgn-np:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_assertion;
    np:hasProvenance dgn-np:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_provenance;
    np:hasPublicationInfo dgn-np:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_assertion a np:Assertion .
  
  dgn-np:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_provenance a np:Provenance .
  
  dgn-np:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0476089 a ncit:C7057 .
  
  dgn-gda:DGNd40555aa6fbd321bf496c0372aba0714 sio:SIO_000628 miriam-gene:1312, lld:C0476089;
    a sio:SIO_001122 .
}

dgn-np:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_provenance {
  dgn-np:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_assertion dcterms:description
      "[Our data suggest, that the CYP1B1 Ser allele may decrease endometrial cancer risk by altering the production of catechol estrogens. However, further studies are warranted to elucidate the role of CYP1B1 in endometrial cancer.]. 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:14656940;
    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:NP59925.RAvWbD00bxow4VVVOvmbWUbp3UjNBqVVtpw7_2jXWWrtQ130_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" .
}