@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA> .
@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:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_head {
  this: np:hasAssertion dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_assertion;
    np:hasProvenance dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_provenance;
    np:hasPublicationInfo dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_assertion a np:Assertion .
  
  dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_provenance a np:Provenance .
  
  dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0018801 a ncit:C7057 .
  
  dgn-gda:DGN03070dbabf01c622b71aa5656d0e43dd sio:SIO_000628 miriam-gene:4846, lld:C0018801;
    a sio:SIO_001122 .
}

dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_provenance {
  dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_assertion dcterms:description
      "[Our data show in failing human myocardium that the T(-786)--&gt;C promoter polymorphism is associated with reduced eNOS expression, whereas the G(894)--&gt;T polymorphism of exon 7 is not associated with change in either eNOS mRNA or protein expression. Reduced eNOS expression associated with the promoter polymorphism may contribute to the vascular, contractile, and autonomic responses to ventricular failure.]. 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:20350698;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:33+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" .
}