@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc> .
@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:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_head {
  this: np:hasAssertion dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_assertion;
    np:hasProvenance dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_provenance;
    np:hasPublicationInfo dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_assertion a np:Assertion .
  
  dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_provenance a np:Provenance .
  
  dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_assertion {
  miriam-gene:673 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNcaa2595c44c2673d3c1462fe3347fcae sio:SIO_000628 miriam-gene:673, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_provenance {
  dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_assertion dcterms:description
      "[BRAF mutation testing has a role in (1) differentiating sporadic colorectal cancer from Lynch syndrome, (2) identifying cancers lacking BRAF mutation that are more likely to respond to epidermal growth factor receptor inhibitor therapy, and (3) conferring worse prognosis in colorectal cancer that is microsatellite stable.]. 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:20670148;
    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:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}