Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Be86ff9eed0b11b458ea22be56ac2830d> ?p ?o ?g. }
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- Be86ff9eed0b11b458ea22be56ac2830d NCIT_P378 "NCI" @default.
- Be86ff9eed0b11b458ea22be56ac2830d type Axiom @default.
- Be86ff9eed0b11b458ea22be56ac2830d annotatedProperty IAO_0000115 @default.
- Be86ff9eed0b11b458ea22be56ac2830d annotatedSource NCIT_C157449 @default.
- Be86ff9eed0b11b458ea22be56ac2830d annotatedTarget "An autosomal dominant tumor syndrome caused by germline CDKN1B mutations that result in a phenotype similar to that of multiple endocrine neoplasia type 1, characterized by endocrine neoplasms, particularly in the parathyroid glands, pituitary, and pancreas. (WHO 2017)" @default.