Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8f0d5a9e239daf87cf1a80932239f285> ?p ?o ?g. }
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- B8f0d5a9e239daf87cf1a80932239f285 hasDbXref "MESH:D046768" @default.
- B8f0d5a9e239daf87cf1a80932239f285 type Axiom @default.
- B8f0d5a9e239daf87cf1a80932239f285 annotatedProperty IAO_0000115 @default.
- B8f0d5a9e239daf87cf1a80932239f285 annotatedSource MONDO_0005803 @default.
- B8f0d5a9e239daf87cf1a80932239f285 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.