@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q> .
@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:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_head {
  this: np:hasAssertion dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_assertion;
    np:hasProvenance dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_provenance;
    np:hasPublicationInfo dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_assertion a np:Assertion .
  
  dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_provenance a np:Provenance .
  
  dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_assertion {
  miriam-gene:4893 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNdbef0785add4a936797be4c16e12f386 sio:SIO_000628 miriam-gene:4893, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_provenance {
  dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_assertion dcterms:description
      "[This review will focus on mutations in genes encoding proteins that play a role in the MAPK pathway and that have been implicated in melanoma biology, such as BRAF, NRAS, and MEK (MAPK kinase), and detail the current understanding of their role in melanoma progression from a molecular biology perspective.]. 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:23752084;
    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:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:28+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" .
}