Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_provenance.
- NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_assertion wasGeneratedBy ECO_0000218 NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_provenance.
- NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_assertion wasDerivedFrom ctd_human-20150221 NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_provenance.
- NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_assertion SIO_000772 15579781 NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_provenance.
- NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_assertion evidence source_evidence_curated NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_provenance.
- NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_assertion description "[Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5436.RA2LGbvAzLI_4_twIBkMdNR33Pg6UybRZgbKj9Rf1OWVA130_provenance.