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- B6a5d5eca531fba7fbfb08079c5389ac1 NCIT_P378 "NCI" @default.
- B6a5d5eca531fba7fbfb08079c5389ac1 type Axiom @default.
- B6a5d5eca531fba7fbfb08079c5389ac1 annotatedProperty IAO_0000115 @default.
- B6a5d5eca531fba7fbfb08079c5389ac1 annotatedSource NCIT_C126870 @default.
- B6a5d5eca531fba7fbfb08079c5389ac1 annotatedTarget "A congenital disorder of glycosylation sub-type caused by mutation(s) in the ALG3 gene, encoding dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase." @default.