@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo> .
@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:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_head {
  this: np:hasAssertion dgn-np:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_assertion;
    np:hasProvenance dgn-np:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_provenance;
    np:hasPublicationInfo dgn-np:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_assertion a np:Assertion .
  
  dgn-np:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_provenance a np:Provenance .
  
  dgn-np:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_assertion {
  miriam-gene:26479 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGN3e487f96baf4f07383494437e5180d4c sio:SIO_000628 miriam-gene:26479, lld:C0011847;
    a sio:SIO_001121 .
}

dgn-np:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_provenance {
  dgn-np:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_assertion dcterms:description
      "[Among obese men, after adjustment for age, duration of diabetes and major lifestyle factors, the CT or TT genotype was associated with an increased CHD risk compared with the CC genotype (odds ratio [OR] 2.52, 95% CI 1.08-5.90); the corresponding ORs (95% CI) were 0.99 (0.58, 1.69) for overweight men (25< or =BMI <30 kg/m(2)) and 0.37 (0.17, 0.79) for lean men (BMI <25 kg/m(2)) (p for interaction 0.001).]. 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:16570154;
    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:NP584642.RAvNgGbSkS9X1nXxNn-_SN2r_cm8gF3XrDYGxaMHONYyo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:52+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" .
}