Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_provenance.
- NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_assertion description "[Hyperinsulinism/ hyperammonemia (HI/HA) syndrome is caused by excessive activity of glutamate dehydrogenase (GDH) encoded by GLUD1 gene, which oxidizes glutamate to alpha-ketoglutarate and which is a potential regulator of insulin secretion in pancreatic beta cells and of ureagenesis in the liver.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_provenance.
- NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_assertion evidence source_evidence_literature NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_provenance.
- NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_assertion SIO_000772 20857847 NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_provenance.
- NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_assertion wasDerivedFrom befree-20150227 NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_provenance.
- NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_assertion wasGeneratedBy ECO_0000203 NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP433893.RA0yeEerGtcsKzl1J08fP6dpvHblY6ZX8lxv4oauJ-mqg130_provenance.