@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo> .
@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:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_head {
  this: np:hasAssertion dgn-np:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_assertion;
    np:hasProvenance dgn-np:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_provenance;
    np:hasPublicationInfo dgn-np:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_assertion a np:Assertion .
  
  dgn-np:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_provenance a np:Provenance .
  
  dgn-np:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0085580 a ncit:C7057 .
  
  dgn-gda:DGN28b96f23fda616a5c6dd4bf22df6153d sio:SIO_000628 miriam-gene:4846, lld:C0085580;
    a sio:SIO_001122 .
}

dgn-np:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_provenance {
  dgn-np:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_assertion dcterms:description
      "[Evidence for the involvement of eNOS single nucleotide polymorphisms in the development of essential hypertension is limited, though the eNOS Glu298Asp polymorphism appears to influence the blood pressure response to exercise.]. 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:12530931;
    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:NP380488.RAd_93jorjfgvtkRuGHNMKD1JtI-h3XMVZD_fhhNvcEuo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:37+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" .
}