@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac> .
@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:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_head {
  this: np:hasAssertion dgn-np:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_assertion;
    np:hasProvenance dgn-np:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_provenance;
    np:hasPublicationInfo dgn-np:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_assertion a np:Assertion .
  
  dgn-np:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_provenance a np:Provenance .
  
  dgn-np:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_assertion {
  miriam-gene:185 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGNa6b1e39480c0afce0f595ea2c597780b sio:SIO_000628 miriam-gene:185, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_provenance {
  dgn-np:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_assertion dcterms:description
      "[These results suggest that the AGT and AT1 receptor genes are not major genetic determinants of hypertension associated with NIDDM in this population, although we can not exclude the possibility that these loci make a minor contribution in a polygenic context.]. 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:9218178;
    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:NP659407.RAj7fjUKlh5f_gNlAP-NDcrMJEBQbmYGuqSlgqaBZdyac130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:38+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}