@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4> .
@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:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_head {
  this: np:hasAssertion dgn-np:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_assertion ;
    np:hasProvenance dgn-np:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_provenance ;
    np:hasPublicationInfo dgn-np:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_assertion a np:Assertion .
  dgn-np:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_provenance a np:Provenance .
  dgn-np:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_assertion {
  miriam-gene:145741 a ncit:C16612 .
  lld:C0011860 a ncit:C7057 .
  dgn-gda:DGNb1b819874d17c4756e686a5ee92f6a99 sio:SIO_000628 miriam-gene:145741 , lld:C0011860 ;
    a sio:SIO_001122 .
}
dgn-np:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_provenance {
  dgn-np:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_assertion dcterms:description "[Our study represents the first GWAS of T2D with both discovery and replication sample sets recruited from Han Chinese men and women residing in Mainland China. We confirmed the associations of KCNQ1 and C2CD4A/B with T2D, with the latter for the first time being examined in Han Chinese. Arguably, eight more independent loci were replicated in our GWAS.]. 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:21799836 ;
    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:NP85017.RARyYxfS1eV-VwxAmifv7AiQ0gBNLsHOqtSQLXIJgMOz4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+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" .
}