Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_assertion> ?p ?o ?g. }
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- NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_assertion type Assertion NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_head.
- NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_assertion wasGeneratedBy ECO_0000218 NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_provenance.
- NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_assertion wasDerivedFrom uniprot-20150221 NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_provenance.
- NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_assertion SIO_000772 9727001 NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_provenance.
- NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_assertion evidence source_evidence_curated NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_provenance.
- NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_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." NP2669.RAR_tRPTJtZK16p1x57tscDbKcb9PaLNw2S2iWf65PLdU130_provenance.