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- B96821c934d7e8cb0f6cda96941fd60f7 NCIT_P378 "NCI" @default.
- B96821c934d7e8cb0f6cda96941fd60f7 type Axiom @default.
- B96821c934d7e8cb0f6cda96941fd60f7 annotatedProperty IAO_0000115 @default.
- B96821c934d7e8cb0f6cda96941fd60f7 annotatedSource NCIT_C201082 @default.
- B96821c934d7e8cb0f6cda96941fd60f7 annotatedTarget "Human DYM wild-type allele is located in the vicinity of 18q21.1 and is approximately 425 kb in length. This allele, which encodes dymeclin protein, plays a role in the organization the Golgi apparatus. Mutation of the gene is associated with Dyggve-Melchior-Clausen syndrome and Smith-McCort dysplasia." @default.