@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E> .
@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 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:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_head {
  this: np:hasAssertion dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_assertion ;
    np:hasProvenance dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_provenance ;
    np:hasPublicationInfo dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_assertion a np:Assertion .
  dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_provenance a np:Provenance .
  dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_assertion {
  miriam-gene:3784 a ncit:C16612 .
  lld:C0011860 a ncit:C7057 .
  dgn-gda:DGN70a0e8e8c25e308eec0f24386960f505 sio:SIO_000628 miriam-gene:3784 , lld:C0011860 ;
    a sio:SIO_001122 .
}
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_provenance {
  dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_assertion dct:description "[We observed numerous regions with suggestive associations with type 2 diabetes. Some of these signals correspond to regions described in previous studies. However, many of these regions could not be replicated in the DIAGRAM datasets. It is critical to carry out additional studies in Hispanic and American Indian populations, which have a high prevalence of type 2 diabetes.]. 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:21573907 ;
    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:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_publicationInfo {
  this: dct:created "2014-10-02T12:32:34+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}