@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w> .
@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:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_head {
  this: np:hasAssertion dgn-np:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_assertion;
    np:hasProvenance dgn-np:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_provenance;
    np:hasPublicationInfo dgn-np:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_assertion a np:Assertion .
  
  dgn-np:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_provenance a np:Provenance .
  
  dgn-np:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_assertion {
  miriam-gene:369 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNea3cb42e92aae24d1354a0610affa964 sio:SIO_000628 miriam-gene:369, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_provenance {
  dgn-np:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_assertion dcterms:description
      "[Our data indicate that, in contrast to the BRAF gene, the ARAF gene is rarely mutated in human cancers, and suggest that alterations of the RAS pathway by ARAF gene mutation may not play an important role in the pathogenesis of human cancers.]. 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:15676015;
    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:NP621468.RAaA6o8-o2eZEg1jurJp7CLCN1iDiumsNaRkQr15emb_w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:15+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" .
}