Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_provenance.
- NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_assertion wasGeneratedBy ECO_0000218 NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_provenance.
- NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_assertion wasDerivedFrom uniprot-2016 NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_provenance.
- NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_assertion SIO_000772 16332676 NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_provenance.
- NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_assertion evidence source_evidence_curated NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_provenance.
- NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_assertion description "[A novel KCNJ11 mutation associated with congenital hyperinsulinism reduces the intrinsic open probability of beta-cell ATP-sensitive potassium channels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4305.RAJhaoa0nFS0RLIwPM6CxJiFbK0VHsLwcUjG6ETbLhLGU130_provenance.