@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w> .
@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:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_head {
  this: np:hasAssertion dgn-np:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_assertion;
    np:hasProvenance dgn-np:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_provenance;
    np:hasPublicationInfo dgn-np:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_assertion a np:Assertion .
  
  dgn-np:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_provenance a np:Provenance .
  
  dgn-np:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_assertion {
  miriam-gene:10561 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNfc7157d23a5cd8b2ca1ef0d1f85a6eb7 sio:SIO_000628 miriam-gene:10561, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_provenance {
  dgn-np:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_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:NP157630.RAUpmkztIJ3f4NxkP58dCEK4qfym59WMS-D_8D9eD9r0w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:25+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" .
}