Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance.
- NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance.
- NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_assertion evidence source_evidence_literature NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance.
- NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_assertion SIO_000772 9648840 NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance.
- NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_assertion wasDerivedFrom befree-2016 NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance.
- NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_assertion wasGeneratedBy ECO_0000203 NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance.