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- Bb83197b55c60c32ff6aa04c41a6ce4b9 NCIT_P378 "NCI" @default.
- Bb83197b55c60c32ff6aa04c41a6ce4b9 type Axiom @default.
- Bb83197b55c60c32ff6aa04c41a6ce4b9 annotatedProperty IAO_0000115 @default.
- Bb83197b55c60c32ff6aa04c41a6ce4b9 annotatedSource NCIT_C189281 @default.
- Bb83197b55c60c32ff6aa04c41a6ce4b9 annotatedTarget "An autosomal recessive condition caused by mutation(s) in the CP gene, encoding ceruloplasmin. It is characterized by low concentrations of ceruloplasmin." @default.