Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_provenance.
- NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_assertion description "[Congenital hyperinsulinism is associated with mutations of SUR-1 and Kir6.2, glucokinase, glutamate dehydrogenase, short-chain 3-hydroxyacyl-CoA dehydrogenase, and ectopic expression on beta-cell plasma membrane of SLC16A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_provenance.
- NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_assertion evidence source_evidence_literature NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_provenance.
- NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_assertion SIO_000772 18156285 NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_provenance.
- NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_assertion wasDerivedFrom befree-20150227 NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_provenance.
- NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_assertion wasGeneratedBy ECO_0000203 NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_provenance.