@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs> .
@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:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_head {
  this: np:hasAssertion dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_assertion;
    np:hasProvenance dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_provenance;
    np:hasPublicationInfo dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_assertion a np:Assertion .
  
  dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_provenance a np:Provenance .
  
  dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN1a610ea84ec48d1fbdcf1225b20cdde0 sio:SIO_000628 miriam-gene:4846, lld:C0007222;
    a sio:SIO_001121 .
}

dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_provenance {
  dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_assertion dcterms:description
      "[Endothelial nitric oxide synthase (eNOS) gene polymorphisms have been associated with the pathogenesis of cardiovascular diseases, but few studies have evaluated the role of eNOS haplotypes on the risk and prognosis of heart failure (HF).]. 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:22290017;
    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:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:58+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" .
}