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- B26481cafa8034053d6a90c05ee463f5c NCIT_P378 "NCI" @default.
- B26481cafa8034053d6a90c05ee463f5c type Axiom @default.
- B26481cafa8034053d6a90c05ee463f5c annotatedProperty IAO_0000115 @default.
- B26481cafa8034053d6a90c05ee463f5c annotatedSource NCIT_C131567 @default.
- B26481cafa8034053d6a90c05ee463f5c annotatedTarget "Human SCN5A wild-type allele is located in the vicinity of 3p21 and is approximately 102 kb in length. This allele, which encodes sodium channel protein type 5 subunit alpha protein, plays a role in voltage-dependent sodium transport. Mutation of the gene is associated with long QT syndrome-3, sick sinus syndrome 1, Brugada syndrome 1, familial atrial fibrillation 10, familial ventricular fibrillation 1, dialated cardiomyopathy 1E, progressive heart block type 1A and non-progressive heart block." @default.