@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k> .
@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:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_head {
  this: np:hasAssertion dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_assertion;
    np:hasProvenance dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_provenance;
    np:hasPublicationInfo dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_assertion a np:Assertion .
  
  dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_provenance a np:Provenance .
  
  dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_assertion {
  miriam-gene:116519 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGN5864b27ef83ce0bd17eb7c8869d81687 sio:SIO_000628 miriam-gene:116519, lld:C0038454;
    a sio:SIO_001121 .
}

dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_provenance {
  dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_assertion dcterms:description
      "[Multiplex regression analysis model adjusted for age, gender, serum total cholesterol levels, acute myocardial infarction and stroke events revealed that the examined ApoA5 variant confers risk for the development of metabolic syndrome: the odds ratio at 95% confidence interval was 3.622 (1.200-10.936), p=0.02.]. 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:17922054;
    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:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:30+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" .
}