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- B99e6fbb72abab948890eeaae00cdc79f hasDbXref "MESH:D046768" @default.
- B99e6fbb72abab948890eeaae00cdc79f type Axiom @default.
- B99e6fbb72abab948890eeaae00cdc79f annotatedProperty IAO_0000115 @default.
- B99e6fbb72abab948890eeaae00cdc79f annotatedSource MONDO_0005803 @default.
- B99e6fbb72abab948890eeaae00cdc79f annotatedTarget "An inherited autosomal recessive syndrome characterized by the disorganized formation of new islets in the pancreas and congenital hyperinsulinism. It is due to focal hyperplasia of pancreatic islet cells budding off from the ductal structures and forming new islets of langerhans. Mutations in the islet cells involve the potassium channel gene kcnj11 or the atp-binding cassette transporter gene abcc8, both on chromosome 11." @default.