dgn-np:NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance {
  dgn-np:NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_assertion dcterms:description "[However, four DR4-DQ beta 3.2 haplotypes that lack DX alpha-TaqI-2.2kb were encountered, two of which are 'affected.' These haplotypes suggest that the identification of the 'disease locus' can be facilitated by the study of unusual haplotypes in which distinct IDDM-associated alleles occur separated from their neighbors of the standard genetic configurations.]. 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:2563360 ;
    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 .
}