@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ> .
@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:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_head {
  this: np:hasAssertion dgn-np:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_assertion;
    np:hasProvenance dgn-np:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_provenance;
    np:hasPublicationInfo dgn-np:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_assertion a np:Assertion .
  
  dgn-np:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_provenance a np:Provenance .
  
  dgn-np:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_assertion {
  miriam-gene:23209 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN6afde5068497c0a3f86fb57c3bc27558 sio:SIO_000628 miriam-gene:23209, lld:C0007222;
    a sio:SIO_001121 .
}

dgn-np:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_provenance {
  dgn-np:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_assertion dcterms:description
      "[Because high-normal blood pressure (BP) confers an increased risk for the development of hypertension and other cardiovascular disorders, including left ventricular hypertrophy (LVH), we tested the hypothesis that the allelic variation (894T) in the eNOS gene would directly correlate with alterations in LV mass (LVM) in individuals with high-normal BP.]. 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:15712782;
    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:NP747869.RAZ0VJtINhdfUoYG1QIAX-4GJPm4cW9YWJnyfcDRaSOgQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:33+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" .
}