@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0> .
@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:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_head {
  this: np:hasAssertion dgn-np:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_assertion;
    np:hasProvenance dgn-np:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_provenance;
    np:hasPublicationInfo dgn-np:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_assertion a np:Assertion .
  
  dgn-np:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_provenance a np:Provenance .
  
  dgn-np:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_assertion {
  miriam-gene:7422 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGNac0a56023abade9d3c2d3ef6bc807073 sio:SIO_000628 miriam-gene:7422, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_provenance {
  dgn-np:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_assertion dct:description
      "[The phenotype based risk models provided greater discrimination for type 2 diabetes than did models based on 20 common independently inherited diabetes risk alleles. The addition of genotypes to phenotype based risk models produced only minimal improvement in accuracy of risk estimation assessed by recalibration and, at best, a minor net reclassification improvement. The major translational application of the currently known common, small effect genetic variants influencing susceptibility to type 2 diabetes is likely to come from the insight they provide on causes of disease and potential therapeutic targets.]. 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:20075150;
    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:NP59141.RAxKRSUk18VE1P5ItlM3_9s6uVhsa5WCHLTYKRDlwiOl0130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+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" .
}