@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0> .
@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:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_head {
  this: np:hasAssertion dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_assertion;
    np:hasProvenance dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_provenance;
    np:hasPublicationInfo dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_assertion a np:Assertion .
  
  dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_provenance a np:Provenance .
  
  dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_assertion {
  miriam-gene:92086 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN2fc6141b49f48603d575d1b0067e43a8 sio:SIO_000628 miriam-gene:92086, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_provenance {
  dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_assertion dcterms:description
      "[These results did not support the hypothesis that the interaction between the T393C polymorphism and GGT in the association with hypertension could be caused by an indirect effect of Gs proteins mediated by glucose metabolism.]. 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:15894831;
    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:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:40+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" .
}