Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B0505d47fe1a9c2050163b697fe4f2d7f> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B0505d47fe1a9c2050163b697fe4f2d7f NCIT_P378 "NCI" @default.
- B0505d47fe1a9c2050163b697fe4f2d7f type Axiom @default.
- B0505d47fe1a9c2050163b697fe4f2d7f annotatedProperty IAO_0000115 @default.
- B0505d47fe1a9c2050163b697fe4f2d7f annotatedSource NCIT_C75467 @default.
- B0505d47fe1a9c2050163b697fe4f2d7f 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.