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- B3bdc065e5c1b056abf32fc7876e8b279 NCIT_P378 "NCI" @default.
- B3bdc065e5c1b056abf32fc7876e8b279 type Axiom @default.
- B3bdc065e5c1b056abf32fc7876e8b279 annotatedProperty IAO_0000115 @default.
- B3bdc065e5c1b056abf32fc7876e8b279 annotatedSource NCIT_C61260 @default.
- B3bdc065e5c1b056abf32fc7876e8b279 annotatedTarget "An X-linked, inherited lysosomal storage disease caused by the deficiency of the enzyme iduronate sulfatase that is responsible for the degradation of mucopolysaccharides. It nearly always affects males and is characterized by the accumulation of mucopolysaccharides in various organs, resulting in mental dysfunction, enlarged abdomen, hearing loss, obstructive airway disease, heart disease, and hepatosplenomegaly." @default.