Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_provenance.
- NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_assertion wasGeneratedBy ECO_0000218 NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_provenance.
- NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_assertion wasDerivedFrom uniprot-2016 NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_provenance.
- NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_assertion SIO_000772 9727001 NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_provenance.
- NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_assertion evidence source_evidence_curated NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_provenance.
- NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_assertion description "[A hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9857.RATO64dO2uQiRBXHjRb1DONTvkRXpPPChrYCHYcsIJFqE130_provenance.