Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_assertion> ?p ?o ?g. }
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- NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_assertion type Assertion NP420921.RAbI-XmQsoijtvT2Tv4xiDc7Q5sz-n89pUiz1By-QCt8U130_head.
- 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.