Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_assertion> ?p ?o ?g. }
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- NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_assertion type Assertion NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_head.
- NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4?) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_provenance.
- NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_assertion evidence source_evidence_literature NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_provenance.
- NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_assertion SIO_000772 21186003 NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_provenance.
- NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_assertion wasDerivedFrom befree-20140225 NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_provenance.
- NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_assertion wasGeneratedBy ECO_0000203 NP882610.RAhpFB6W6kA3nHtHVyViL8gY-fzOGEuQARh9MUNFE1nug130_provenance.