Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance.
- NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_assertion 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." NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance.
- NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_assertion evidence source_evidence_literature NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance.
- NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_assertion SIO_000772 2563360 NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance.
- NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_assertion wasDerivedFrom befree-20150227 NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance.
- NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_assertion wasGeneratedBy ECO_0000203 NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP366460.RAnHuCXimC0kUyPjtDEIl7YQNU3zw0TPzM-Sd2RSF1FXQ130_provenance.