@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo> .
@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/v4.0.0/void/> .

dgn-np:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_head {
  this: np:hasAssertion dgn-np:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_assertion;
    np:hasProvenance dgn-np:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_provenance;
    np:hasPublicationInfo dgn-np:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_assertion a np:Assertion .
  
  dgn-np:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_provenance a np:Provenance .
  
  dgn-np:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_assertion {
  miriam-gene:673 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGN306989da06cc864d73477a242afded0f sio:SIO_000628 miriam-gene:673, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_provenance {
  dgn-np:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_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-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP535633.RAcgXdR8IQrigfX92qAPEsVEJgff38Vm6pGH_7TYXhSmo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:47+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}