@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0> .
@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:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_head {
  this: np:hasAssertion dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_assertion;
    np:hasProvenance dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_provenance;
    np:hasPublicationInfo dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_assertion a np:Assertion .
  
  dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_provenance a np:Provenance .
  
  dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_assertion {
  miriam-gene:7391 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGNe76ff313a46ad350516d9c8ca4095ab2 sio:SIO_000628 miriam-gene:7391, lld:C0524620;
    a sio:SIO_001122 .
}

dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_provenance {
  dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_assertion dc:description
      "[Seven APOA5 single nucleotide polymorphisms (SNPs) were analyzed in combination with six USF1 SNPs, applying logistic regression in an additive model adjusting for age and sex and the definition for metabolic syndrome from the National Cholesterol Education Program's Adult Treatment Panel III (NCEP (AIII)) including medication.]. 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:20054229;
    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:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_publicationInfo {
  this: dc:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}