Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B952bf58cc406c78ef3872f92c424ce5e> ?p ?o ?g. }
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- B952bf58cc406c78ef3872f92c424ce5e NCIT_P378 "NCI" @default.
- B952bf58cc406c78ef3872f92c424ce5e type Axiom @default.
- B952bf58cc406c78ef3872f92c424ce5e annotatedProperty IAO_0000115 @default.
- B952bf58cc406c78ef3872f92c424ce5e annotatedSource NCIT_C75467 @default.
- B952bf58cc406c78ef3872f92c424ce5e annotatedTarget "An inherited degenerative disorder involving the peripheral nerves. It is caused by mutations in the genes that are responsible for the production of proteins necessary for the function and structure of the peripheral nerves. It is characterized by muscle atrophy and weakness in the feet, legs, hands, and arms and loss of sensation in the limbs." @default.