Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B7a17e1f11ed1d489bfe716b1a45a5722> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B7a17e1f11ed1d489bfe716b1a45a5722 NCIT_P378 "NCI" @default.
- B7a17e1f11ed1d489bfe716b1a45a5722 type Axiom @default.
- B7a17e1f11ed1d489bfe716b1a45a5722 annotatedProperty IAO_0000115 @default.
- B7a17e1f11ed1d489bfe716b1a45a5722 annotatedSource NCIT_C175955 @default.
- B7a17e1f11ed1d489bfe716b1a45a5722 annotatedTarget "A cytogenetic abnormality that refers to the duplication of all or part of the long arm of chromosome 16." @default.