@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE> .
@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:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_head {
  this: np:hasAssertion dgn-np:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_assertion;
    np:hasProvenance dgn-np:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_provenance;
    np:hasPublicationInfo dgn-np:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_assertion a np:Assertion .
  
  dgn-np:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_provenance a np:Provenance .
  
  dgn-np:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_assertion {
  miriam-gene:23564 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN86384d5126036cf459ed6c37213abe34 sio:SIO_000628 miriam-gene:23564, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_provenance {
  dgn-np:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_assertion dcterms:description
      "[The association study of G(-6)A, A(-20)C and M235T variants in 111 hypertensives with strong family history and 190 normotensives with no family history showed significant linkage disequilibrium between particular haplotypes, but we could find no association with hypertension.]. 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:10528248;
    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:NP884642.RAIzv_YTtxN7mrsO7hGBAHJ0JpiXXPJaYf10tdyHgMqlE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:00+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" .
}