Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_provenance.
- NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_assertion description "[Mutations in the pancreatic ATP sensitive K(+) channel proteins [sulfonyluea receptor 1 (SUR1) and inward rectifier K(+) channel Kir6.2 (Kir6.2), encoded by ATP-binding cassette transporter subfamily C member 8 (ABCC8) and potassium channel J11 (KCNJ11), respectively], are the most common cause of neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_provenance.
- NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_assertion evidence source_evidence_literature NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_provenance.
- NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_assertion SIO_000772 22831748 NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_provenance.
- NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_assertion wasDerivedFrom befree-20140225 NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_provenance.
- NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_assertion wasGeneratedBy ECO_0000203 NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP922953.RA241e1locjwQbNzyqCOOrwq81qcgXaEqCzobNdjuUh1Y130_provenance.