@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA> .
@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:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_head {
  this: np:hasAssertion dgn-np:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_assertion;
    np:hasProvenance dgn-np:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_provenance;
    np:hasPublicationInfo dgn-np:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_assertion a np:Assertion .
  
  dgn-np:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_provenance a np:Provenance .
  
  dgn-np:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_assertion {
  miriam-gene:2263 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGNa7b0145a18062c79579eef1feb989eb1 sio:SIO_000628 miriam-gene:2263, lld:C1140680;
    a sio:SIO_001122 .
}

dgn-np:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_provenance {
  dgn-np:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_assertion dcterms:description
      "[Despite the low incidence of FGFR2 mutations in ovarian cancer, the two FGFR2 mutations identified in ovarian tumors (S252W, Y376C) overlap with the oncogenic mutations previously identified in endometrial tumors, suggesting activated FGFR2 may contribute to ovarian cancer pathogenesis in a small subset of ovarian tumors.]. 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:20106510;
    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:NP87689.RA_8DfvlpVhle8FLqBgcd7oItLMcBwvcvhP2nMQhpJfDA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:43+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" .
}