@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY> .
@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:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_head {
  this: np:hasAssertion dgn-np:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_assertion;
    np:hasProvenance dgn-np:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_provenance;
    np:hasPublicationInfo dgn-np:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_assertion a np:Assertion .
  
  dgn-np:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_provenance a np:Provenance .
  
  dgn-np:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGNc74da8914cee6221fa73257c222babb9 sio:SIO_000628 miriam-gene:4846, lld:C0011847;
    a sio:SIO_001122 .
}

dgn-np:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_provenance {
  dgn-np:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_assertion dcterms:description
      "[To determine the frequency of eNOS G894T variant and to find the possible association between this polymorphism with CAD we studied 207 unrelated patients with total CAD (with and without diabetes) and 92 controls.]. 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:21602253;
    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:NP895892.RA2Fmh3UfNmz9BhopqBxQ04O2GCQNPJxFWGOUyjnpBOzY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:30+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" .
}