@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q> .
@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:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_head {
  this: np:hasAssertion dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_assertion;
    np:hasProvenance dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_provenance;
    np:hasPublicationInfo dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_assertion a np:Assertion .
  
  dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_provenance a np:Provenance .
  
  dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_assertion {
  miriam-gene:5468 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN981ad1631eab4285f434452019af3ff9 sio:SIO_000628 miriam-gene:5468, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_provenance {
  dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_assertion dcterms:description
      "[The PPARgamma-2 genotype was not associated with an increased or reduced risk of the occurrence of CHD and can therefore not be regarded as an independent risk factor for CHD in patients with diabetes mellitus.]. 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:11916624;
    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:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:56+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" .
}