@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8> .
@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:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_head {
  this: np:hasAssertion dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_assertion;
    np:hasProvenance dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_provenance;
    np:hasPublicationInfo dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_assertion a np:Assertion .
  
  dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_provenance a np:Provenance .
  
  dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_assertion {
  miriam-gene:673 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN9c7c2dd4e43ce549e3709130dbb7352b sio:SIO_000628 miriam-gene:673, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_provenance {
  dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_assertion dcterms:description
      "[The association of BRAF V600E mutation and the presence of the CpG island methylator phenotype (CIMP) and microsatellite instability (MSI) often confound analysis of BRAF mutation status and survival in colorectal carcinoma.]. 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:22314188;
    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:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:46+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" .
}