Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bcfd2e964308d8ccf73a13968e110a2c9> ?p ?o ?g. }
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- Bcfd2e964308d8ccf73a13968e110a2c9 hasDbXref "Orphanet:614" @default.
- Bcfd2e964308d8ccf73a13968e110a2c9 type Axiom @default.
- Bcfd2e964308d8ccf73a13968e110a2c9 annotatedProperty IAO_0000115 @default.
- Bcfd2e964308d8ccf73a13968e110a2c9 annotatedSource MONDO_0009710 @default.
- Bcfd2e964308d8ccf73a13968e110a2c9 annotatedTarget "A rare, genetic, skeletal muscle channelopathy characterized by slow muscle relaxation after contraction (myotonia)." @default.