Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_assertion> ?p ?o ?g. }
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- NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_assertion type Assertion NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_head.
- NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_assertion description "[Recent evidence suggests that mutations in HADH cause HH that is precipitated by protein in a similar manner to the hyperinsulinism/hyperammonemia (HI/HA) syndrome, which is caused by mutations in the GLUD1 gene, encoding the enzyme glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_provenance.
- NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_assertion evidence source_evidence_literature NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_provenance.
- NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_assertion SIO_000772 23253615 NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_provenance.
- NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_assertion wasDerivedFrom befree-2016 NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_provenance.
- NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_assertion wasGeneratedBy ECO_0000203 NP1037372.RAWKMhv_Xm7C3KELP1hb74vkarRTta5APFDCecT2tfEls130_provenance.