@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg> .
@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:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_head {
  this: np:hasAssertion dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_assertion;
    np:hasProvenance dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_provenance;
    np:hasPublicationInfo dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_assertion a np:Assertion .
  
  dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_provenance a np:Provenance .
  
  dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
  dgn-gda:DGN1411e7c7a83fcf91aef5ad6b54165e0b sio:SIO_000628 miriam-gene:3845, lld:C0029925;
    a sio:SIO_001121 .
}

dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_provenance {
  dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_assertion dcterms:description
      "[The goals of this study were to perform a comprehensive assessment of the prevalence of KRAS oncogene mutations in invasive epithelial ovarian carcinomas of various histologic subtypes, and for any subgroup(s) in which KRAS mutation was found to be common, to address the hypothesis that those tumors without KRAS mutation had sustained alternative activation of this signaling pathway through mutation of the BRAF oncogene.]. 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:12893203;
    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:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:32+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" .
}