@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms> .
@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:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_head {
  this: np:hasAssertion dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_assertion;
    np:hasProvenance dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_provenance;
    np:hasPublicationInfo dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_assertion a np:Assertion .
  
  dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_provenance a np:Provenance .
  
  dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_assertion {
  miriam-gene:673 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN1b7121cb0948d6d1f34c07e163bdd5a1 sio:SIO_000628 miriam-gene:673, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_provenance {
  dgn-np:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_assertion dcterms:description
      "[While the frequency of KRAS mutations is comparable with other populations, absence of BRAF mutations is intriguing and would require further analysis of the molecular epidemiology of CRC in West Africa.]. 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:23962701;
    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:NP209671.RAY6HvIMreFxJF3ygWIbEVGWh9H7KHl2wprEgxyiWgRms130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:55+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" .
}