Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bb79f7b98908d1ac2cfbef734d6dcd23f> ?p ?o ?g. }
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- Bb79f7b98908d1ac2cfbef734d6dcd23f hasDbXref "Orphanet:902" @default.
- Bb79f7b98908d1ac2cfbef734d6dcd23f type Axiom @default.
- Bb79f7b98908d1ac2cfbef734d6dcd23f annotatedProperty IAO_0000115 @default.
- Bb79f7b98908d1ac2cfbef734d6dcd23f annotatedSource MONDO_0010196 @default.
- Bb79f7b98908d1ac2cfbef734d6dcd23f annotatedTarget "A rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders." @default.