@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM> .
@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:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_head {
  this: np:hasAssertion dgn-np:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_assertion;
    np:hasProvenance dgn-np:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_provenance;
    np:hasPublicationInfo dgn-np:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_assertion a np:Assertion .
  
  dgn-np:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_provenance a np:Provenance .
  
  dgn-np:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  
  lld:C0206701 a ncit:C7057 .
  
  dgn-gda:DGNbdf94195f53737e8f0aa1436d8475940 sio:SIO_000628 miriam-gene:3845, lld:C0206701;
    a sio:SIO_001121 .
}

dgn-np:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_provenance {
  dgn-np:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_assertion dcterms:description
      "[The molecular genetic findings confirm our hypothesis of dual pathways of serous carcinogenesis based on previous analyses of KRAS and BRAF mutations on the same set of cases in which KRAS and BRAF mutations were found in 60% of SBTs and low-grade serous carcinoma but not in high-grade serous carcinomas.]. 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:15644779;
    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:NP611172.RAg_X4wQgdTUJDGhlysqk3W_VEH9kYoMtZnPQ1hz69vvM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:09+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" .
}