@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI> .
@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:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_head {
  this: np:hasAssertion dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_assertion;
    np:hasProvenance dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_provenance;
    np:hasPublicationInfo dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_assertion a np:Assertion .
  
  dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_provenance a np:Provenance .
  
  dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGN68cd1b76d86d4489c0d684689cf48276 sio:SIO_000628 miriam-gene:4436, lld:C0032580;
    a sio:SIO_001121 .
}

dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_provenance {
  dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_assertion dcterms:description
      "[To clarify the extent of BRAF mutations in HNPCC colorectal carcinomas, which are typical mismatch repair deficient carcinomas, we compared the frequency of BRAF mutations between HNPCC, familial adenomatous polyposis (FAP) and sporadic cases.]. 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:15194222;
    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:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:44+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" .
}