@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k> .
@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:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_head {
  this: np:hasAssertion dgn-np:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_assertion;
    np:hasProvenance dgn-np:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_provenance;
    np:hasPublicationInfo dgn-np:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_assertion a np:Assertion .
  
  dgn-np:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_provenance a np:Provenance .
  
  dgn-np:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_assertion {
  miriam-gene:342977 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN52668a351d668d7b4f587e4c95a6d793 sio:SIO_000628 miriam-gene:342977, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_provenance {
  dgn-np:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_assertion dcterms:description
      "[The association of baseline fitness with risk of hypertension was nominally modified by genotype at markers within the angiotensin converting enzyme, angiotensinogen, BDKRB2 and NOS3 genes in blacks and the BDKRB2, endothelin-1 and PPARGC1A genes in whites.]. 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:20944660;
    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:NP327830.RAA131mdcnlrbaxzpP6AW5jxVWEGNbx6S5FSApddm1h6k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:13+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" .
}