@prefix dct: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8> .
@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:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_head {
  this: np:hasAssertion dgn-np:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_assertion;
    np:hasProvenance dgn-np:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_provenance;
    np:hasPublicationInfo dgn-np:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_assertion a np:Assertion .
  
  dgn-np:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_provenance a np:Provenance .
  
  dgn-np:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_assertion {
  miriam-gene:10205 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN0f9bcd1d4974e7e2624ba3c67b4e0489 sio:SIO_000628 miriam-gene:10205, lld:C0007222;
    a sio:SIO_001121 .
}

dgn-np:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_provenance {
  dgn-np:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_assertion dct:description
      "[Among 11 OTC polymorphisms that were originally selected from databases, the tag single-nucleotide polymorphism (SNP) rs5963409 and the independent SNP rs1800321 were tested for association with hypertension in two independent population samples recruited in Northern (Multinational MONItoring of trends and determinants in CArdiovascular disease (MONICA) study, n = 1,138) and Western (Etude du Vieillissement Artériel (EVA) study, n = 1,166) France.]. 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:19574962;
    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:NP933397.RAEk8Dqa8miiEl0z3oRy6GFJ7upLcnmDREhmr5lIArnE8130_publicationInfo {
  this: dct:created "2014-10-02T12:41:32+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 <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" .
}