@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0> .
@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:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_head {
  this: np:hasAssertion dgn-np:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_assertion;
    np:hasProvenance dgn-np:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_provenance;
    np:hasPublicationInfo dgn-np:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_assertion a np:Assertion .
  
  dgn-np:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_provenance a np:Provenance .
  
  dgn-np:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_assertion {
  miriam-gene:728340 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNa6f19320adbbbdd1be6c5fa5d944f2a9 sio:SIO_000628 miriam-gene:728340, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_provenance {
  dgn-np:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_assertion dcterms:description
      "[On the basis of our data showing that melanoma iNOS expression predicts shortened patient survival, we formulated the hypothesis that activating mutations of NRAS or BRAF, which lead to constitutive activation of the p44/42 MAPK pathway, drive iNOS expression in human melanoma.]. 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:16474847;
    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:NP785780.RAzUlr_aXEdWMj4HXZp-9z08CMo_APeuw2deu1jcrUse0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:56+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" .
}