@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA> .
@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:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_head {
  this: np:hasAssertion dgn-np:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_assertion;
    np:hasProvenance dgn-np:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_provenance;
    np:hasPublicationInfo dgn-np:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_assertion a np:Assertion .
  
  dgn-np:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_provenance a np:Provenance .
  
  dgn-np:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_assertion {
  miriam-gene:9360 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN94b863066e3c6609b3737174fc7ad97e sio:SIO_000628 miriam-gene:9360, lld:C0007222;
    a sio:SIO_001121 .
}

dgn-np:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_provenance {
  dgn-np:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_assertion dcterms:description
      "[Initial epidemiologic studies have demonstrated that genetic variation in the CYP epoxygenase pathway significantly modifies cardiovascular disease risk at the population level in humans, providing support for the hypothesis that modulation of this pathway may represent a novel approach to the prevention and treatment of cardiovascular disease.]. 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:17979511;
    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:NP551401.RAkVEqPkxTQq-GmVIhmTIUxboFtHgNGlHTWHEIgR6BhXA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:32+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" .
}