@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM> .
@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:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_head {
  this: np:hasAssertion dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_assertion;
    np:hasProvenance dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_provenance;
    np:hasPublicationInfo dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_assertion a np:Assertion .
  
  dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_provenance a np:Provenance .
  
  dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN5e64ba5b1f9a190524a3edea8f3c26de sio:SIO_000628 miriam-gene:183, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_provenance {
  dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_assertion dcterms:description
      "[We carried out association studies and multivariate analyses including other candidate causal factors of HP such as the M235T variant of the angiotensinogen (AGT) gene, prepregnancy body mass index (BMI), and family history of hypertension in Japanese subjects.]. 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:15042429;
    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:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}