Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B735546c8b38be0081636519d38e06052> ?p ?o ?g. }
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- B735546c8b38be0081636519d38e06052 NCIT_P378 "NCI" @default.
- B735546c8b38be0081636519d38e06052 type Axiom @default.
- B735546c8b38be0081636519d38e06052 annotatedProperty IAO_0000115 @default.
- B735546c8b38be0081636519d38e06052 annotatedSource NCIT_C185241 @default.
- B735546c8b38be0081636519d38e06052 annotatedTarget "A chromosomal anomaly characterized by the partial duplication of the short arm of chromosome 2. The phenotype is highly variable but principally characterized by growth failure, global developmental delay, facial dysmorphism and ocular anomalies." @default.