@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ> .
@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 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:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_head {
  this: np:hasAssertion dgn-np:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_assertion;
    np:hasProvenance dgn-np:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_provenance;
    np:hasPublicationInfo dgn-np:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_assertion a np:Assertion .
  
  dgn-np:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_provenance a np:Provenance .
  
  dgn-np:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_assertion {
  miriam-gene:1584 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN886ddfcb038fa0352a1e8bfdb3e685c2 sio:SIO_000628 miriam-gene:1584, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_provenance {
  dgn-np:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_assertion dct:description
      "[Our data did not support the association between Mendelian disease gene variants and essential hypertension in the Japanese. However, the present study did not definitively resolve this issue and further investigation is certainly warranted.]. 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:11675945;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}