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- B7bd4c16290de3e4f75ab323fbaac7115 NCIT_P378 "NCI" @default.
- B7bd4c16290de3e4f75ab323fbaac7115 type Axiom @default.
- B7bd4c16290de3e4f75ab323fbaac7115 annotatedProperty IAO_0000115 @default.
- B7bd4c16290de3e4f75ab323fbaac7115 annotatedSource NCIT_C84992 @default.
- B7bd4c16290de3e4f75ab323fbaac7115 annotatedTarget "A rare autosomal recessive inherited disorder caused by mutations in the cathepsin C gene. It is manifested with periodontitis resulting in the premature loss of teeth and palmoplantar keratoderma." @default.