@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM> .
@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:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_head {
  this: np:hasAssertion dgn-np:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_assertion;
    np:hasProvenance dgn-np:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_provenance;
    np:hasPublicationInfo dgn-np:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_assertion a np:Assertion .
  
  dgn-np:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_provenance a np:Provenance .
  
  dgn-np:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_assertion {
  miriam-gene:6934 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGNf53970c7c172bb6128e9f61b28c1416d sio:SIO_000628 miriam-gene:6934, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_provenance {
  dgn-np:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_assertion dcterms:description
      "[Although previous studies showed that the association between the SNP rs7903146 in the TCF7L2 gene and T2D was controversial within the Han Chinese population, we have confirmed the significant association between the SNP rs7903146 in the TCF7L2 gene and T2D in both this study and the meta-analysis in the population.]. 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:20550665;
    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:NP62494.RAH80zYjOkh54b23_DjCfv0VAiUC0fRSwmxtJtDyNyrAM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}