Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B73d0cfc5190e5fc1f21e293c387d7bd0> ?p ?o ?g. }
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- B73d0cfc5190e5fc1f21e293c387d7bd0 hasDbXref "NCIT:C85215" @default.
- B73d0cfc5190e5fc1f21e293c387d7bd0 type Axiom @default.
- B73d0cfc5190e5fc1f21e293c387d7bd0 annotatedProperty IAO_0000115 @default.
- B73d0cfc5190e5fc1f21e293c387d7bd0 annotatedSource MONDO_0700086 @default.
- B73d0cfc5190e5fc1f21e293c387d7bd0 annotatedTarget "A condition characterized by the inheritance of a chromosome pair from one parent and no chromosomal copies from the other parent. It results in developmental abnormalities or rare recessive disorders." @default.