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- B9219e7568cdb9dab79f202c5e1a9c4ce NCIT_P378 "NCI" @default.
- B9219e7568cdb9dab79f202c5e1a9c4ce type Axiom @default.
- B9219e7568cdb9dab79f202c5e1a9c4ce annotatedProperty IAO_0000115 @default.
- B9219e7568cdb9dab79f202c5e1a9c4ce annotatedSource NCIT_C189281 @default.
- B9219e7568cdb9dab79f202c5e1a9c4ce annotatedTarget "An autosomal recessive condition caused by mutation(s) in the CP gene, encoding ceruloplasmin. It is characterized by low concentrations of ceruloplasmin." @default.