Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Badfc78fd3b3abd2fa2ebe7c91a61004c> ?p ?o ?g. }
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- Badfc78fd3b3abd2fa2ebe7c91a61004c NCIT_P378 "NICHD" @default.
- Badfc78fd3b3abd2fa2ebe7c91a61004c type Axiom @default.
- Badfc78fd3b3abd2fa2ebe7c91a61004c annotatedProperty NCIT_P325 @default.
- Badfc78fd3b3abd2fa2ebe7c91a61004c annotatedSource NCIT_C126876 @default.
- Badfc78fd3b3abd2fa2ebe7c91a61004c annotatedTarget "SHOX deficiency due to homozygous mutation(s) in the SHOX gene. This condition is characterized by severe hypoplasia of the radius/ulna and tibia/fibula resulting in extreme short stature." @default.