@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY> .
@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:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_head {
  this: np:hasAssertion dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_assertion;
    np:hasProvenance dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_provenance;
    np:hasPublicationInfo dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_assertion a np:Assertion .
  
  dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_provenance a np:Provenance .
  
  dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_assertion {
  miriam-gene:5241 a ncit:C16612 .
  
  lld:C0677886 a ncit:C7057 .
  
  dgn-gda:DGN03e1962dd97ae6627925ee73fda6fed8 sio:SIO_000628 miriam-gene:5241, lld:C0677886;
    a sio:SIO_001121 .
}

dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_provenance {
  dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_assertion dcterms:description
      "[To assess whether the progesterone receptor (PR) exon 4 valine to leucine amino acid variant is associated with specific tumour characteristics or with overall risk of ovarian cancer, we examined 551 cases of epithelial ovarian cancer and 298 unaffected controls for the underlying G-->T nucleotide substitution polymorphism.]. 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:11323389;
    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:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:20+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" .
}