Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_provenance.
- NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_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." NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_provenance.
- NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_assertion evidence source_evidence_literature NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_provenance.
- NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_assertion SIO_000772 22831748 NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_provenance.
- NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_assertion wasDerivedFrom befree-20150227 NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_provenance.
- NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_assertion wasGeneratedBy ECO_0000203 NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP720505.RApvh-Wg8wCz7dwfRx9llMD9sDlfUVGNMaYYjIf1r7mMk130_provenance.