@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI> .
@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/v3.0.0/void/> .
dgn-np:NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI130_head {
   this: np:hasAssertion dgn-np:NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI130_assertion ;
    np:hasProvenance dgn-np:NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI130_provenance ;
    np:hasPublicationInfo dgn-np:NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI130_provenance a np:Provenance .
  dgn-np:NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI130_assertion {
   miriam-gene:8050 a ncit:C16612 .
  lld:C0011860 a ncit:C7057 .
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    a sio:SIO_001122 .
}
dgn-np:NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI130_provenance {
   dgn-np:NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI130_assertion dcterms:description "[In addition, two missense variants in PAM, encoding p.Asp563Gly (frequency of 4.98%) and p.Ser539Trp (frequency of 0.65%), confer moderately higher risk of T2D (OR = 1.23, P = 3.9 × 10(-10) and OR = 1.47, P = 1.7 × 10(-5), respectively), and a rare (0.20%) frameshift variant in PDX1, encoding p.Gly218Alafs*12, associates with high risk of T2D (OR = 2.27, P = 7.3 × 10(-7)).]. 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:24464100 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP789121.RASaPqL9GLI7RPYHPLcKOUXCNY9EyEogQanFxjlRNdsTI130_publicationInfo {
   this: dcterms:created "2015-08-25T14:45:37+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:disgenetv3.0rdf ;
    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> ;
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}