@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM> .
@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:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_head {
  this: np:hasAssertion dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_assertion;
    np:hasProvenance dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_provenance;
    np:hasPublicationInfo dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_assertion a np:Assertion .
  
  dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_provenance a np:Provenance .
  
  dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_assertion {
  miriam-gene:4842 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_provenance {
  dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_assertion dcterms:description
      "[To analyze the functional significance of the G894T polymorphism of NOS3, the gene encoding endothelial nitric oxide synthase (NOS), we assessed basal nitric oxide activity and the amount of oxidative stress in the renal circulation of patients with type 2 diabetes.]. 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:18622262;
    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:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:29+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" .
}