@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_head {
  this: np:hasAssertion dgn-np:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_assertion ;
    np:hasProvenance dgn-np:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_provenance ;
    np:hasPublicationInfo dgn-np:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_assertion a np:Assertion .
  dgn-np:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_provenance a np:Provenance .
  dgn-np:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_assertion {
  miriam-gene:2645 a ncit:C16612 .
  lld:C0020456 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_provenance {
  dgn-np:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_assertion dcterms:description "[Since glucokinase mutations predominantly induce subclinical hyperglycaemia, it is likely that in the locality of other pedigrees there will be undiagnosed subjects with the same glucokinase mutation, which remains undetected unless pregnancy occurs.]. 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:8932999 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1363062.RAjl-l_glND9EFS7k1sHUPTKTu1m--IDHCLPigYOdvNCU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:04+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}