@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM> .
@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:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_head {
  this: np:hasAssertion dgn-np:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_assertion;
    np:hasProvenance dgn-np:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_provenance;
    np:hasPublicationInfo dgn-np:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_assertion a np:Assertion .
  
  dgn-np:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_provenance a np:Provenance .
  
  dgn-np:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGNc9271cfd7cff9e6b3482cb02063d8b2b sio:SIO_000628 miriam-gene:183, lld:C0007222;
    a sio:SIO_001121 .
}

dgn-np:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_provenance {
  dgn-np:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_assertion dcterms:description
      "[To date, the human angiotensinogen (AGT) gene and some of its variants represent the best examples of genetic influences that are involved in the determination of essential hypertension (EH) and associated cardiovascular diseases (CVDs).]. 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:9831339;
    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:NP219436.RAcKYCpel5J-v8806aJD_1OKLUyArhw9Tc6Vx8uj0WQrM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:01+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" .
}