@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds> .
@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:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_head {
  this: np:hasAssertion dgn-np:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_assertion;
    np:hasProvenance dgn-np:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_provenance;
    np:hasPublicationInfo dgn-np:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_assertion a np:Assertion .
  
  dgn-np:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_provenance a np:Provenance .
  
  dgn-np:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_assertion {
  miriam-gene:4306 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN5d3c0b949dff8e77a45c52cad314a849 sio:SIO_000628 miriam-gene:4306, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_provenance {
  dgn-np:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_assertion dcterms: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:NP53614.RAa_0XD6YsxARQQy8KBBNu5abMJe9SljP_4VZclTEH7ds130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}