Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B2b7be3b0423bc66e11fa3dd73bc56c8a> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B2b7be3b0423bc66e11fa3dd73bc56c8a NCIT_P378 "NCI" @default.
- B2b7be3b0423bc66e11fa3dd73bc56c8a type Axiom @default.
- B2b7be3b0423bc66e11fa3dd73bc56c8a annotatedProperty IAO_0000115 @default.
- B2b7be3b0423bc66e11fa3dd73bc56c8a annotatedSource NCIT_C62505 @default.
- B2b7be3b0423bc66e11fa3dd73bc56c8a annotatedTarget "An autosomal recessive genetic disorder characterized by bone marrow failure, skeletal abnormalities, and an increased incidence of the development of neoplasias." @default.