Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_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." NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_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.
- 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.
- 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." provenance.