@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs> .
@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:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_head {
  this: np:hasAssertion dgn-np:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_assertion;
    np:hasProvenance dgn-np:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_provenance;
    np:hasPublicationInfo dgn-np:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_assertion a np:Assertion .
  
  dgn-np:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_provenance a np:Provenance .
  
  dgn-np:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_assertion {
  miriam-gene:9197 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN0195d9d85945e4c902e1edeafe7d3059 sio:SIO_000628 miriam-gene:9197, lld:C0007222;
    a sio:SIO_001121 .
}

dgn-np:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_provenance {
  dgn-np:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_assertion dcterms:description
      "[The finding of polymorphic sites in the functional promoter of the human AT1 locus will be beneficial to the study of the role of the AT1 receptor gene in hypertension and other cardiovascular diseases.]. 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:10738546;
    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:NP248523.RAUO7KREwKe_wgaPoh6njoOX7P3Pt8olg2371vNmGsJKs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:19+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" .
}