Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bdbe7aedc3446f4b3cf574b705b57fe7c> ?p ?o ?g. }
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- Bdbe7aedc3446f4b3cf574b705b57fe7c NCIT_P378 "NCI" @default.
- Bdbe7aedc3446f4b3cf574b705b57fe7c type Axiom @default.
- Bdbe7aedc3446f4b3cf574b705b57fe7c annotatedProperty IAO_0000115 @default.
- Bdbe7aedc3446f4b3cf574b705b57fe7c annotatedSource NCIT_C153560 @default.
- Bdbe7aedc3446f4b3cf574b705b57fe7c annotatedTarget "A cytogenetic abnormality that refers to any translocation involving Xp11.2 on the short arm of the X chromosome." @default.