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- B70b34be96a7ba51cb47babf39989a4ae NCIT_P378 "NCI" @default.
- B70b34be96a7ba51cb47babf39989a4ae type Axiom @default.
- B70b34be96a7ba51cb47babf39989a4ae annotatedProperty IAO_0000115 @default.
- B70b34be96a7ba51cb47babf39989a4ae annotatedSource NCIT_C84793 @default.
- B70b34be96a7ba51cb47babf39989a4ae annotatedTarget "An autosomal recessive inherited syndrome caused by mutations in the KCNE1 and KCNQ1 genes. It is characterized by congenital hearing loss and arrhythmia. It is a form of long QT syndrome." @default.