Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_assertion type Assertion NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_head.
- NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_assertion wasGeneratedBy ECO_0000218 NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_provenance.
- NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_assertion wasDerivedFrom uniprot-20130724 NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_provenance.
- NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_assertion SIO_000772 9727001 NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_provenance.
- NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_assertion evidence source_evidence_curated NP3447.RASSsa_CH6OkLrK2PT5O9x84vVxob9KRToWullWCkNOig130_provenance.
- 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.