@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_head {
  this: np:hasAssertion dgn-np:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_assertion;
    np:hasProvenance dgn-np:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_provenance;
    np:hasPublicationInfo dgn-np:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_assertion a np:Assertion .
  
  dgn-np:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_provenance a np:Provenance .
  
  dgn-np:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_assertion {
  miriam-gene:6635 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNed7bdb598f64fa2a95b46361ae86128a sio:SIO_000628 miriam-gene:6635, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_provenance {
  dgn-np:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_assertion dcterms:description
      "[B-RAF mutations, predominantly the specific V600E mutation and additional alterations in exons 11 and 15, were frequently detected in malignant melanomas, papillary thyroid tumors, and colorectal cancers with microsatellite instability (MSI).]. 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:16413100;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP705536.RAlByJYVnNdPA1SHFJCCfsLqe3PeyuUXLZzLfV4lrOSPs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:45+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}