Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B03980b5d554238a80922a9636d86d1cf> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B03980b5d554238a80922a9636d86d1cf hasDbXref "NCIT:P378" @default.
- B03980b5d554238a80922a9636d86d1cf type Axiom @default.
- B03980b5d554238a80922a9636d86d1cf annotatedProperty IAO_0000115 @default.
- B03980b5d554238a80922a9636d86d1cf annotatedSource MONDO_0002441 @default.
- B03980b5d554238a80922a9636d86d1cf 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.