Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance.
- NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_assertion wasGeneratedBy ECO_0000218 NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance.
- NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_assertion wasDerivedFrom uniprot-20130724 NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance.
- NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_assertion SIO_000772 15562009 NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance.
- NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_assertion evidence source_evidence_curated NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance.
- NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_assertion description "[Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance.