Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bfb8d1f960d30680489806f209e8bb552> ?p ?o ?g. }
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- Bfb8d1f960d30680489806f209e8bb552 NCIT_P378 "NCI" @default.
- Bfb8d1f960d30680489806f209e8bb552 type Axiom @default.
- Bfb8d1f960d30680489806f209e8bb552 annotatedProperty IAO_0000115 @default.
- Bfb8d1f960d30680489806f209e8bb552 annotatedSource NCIT_C186789 @default.
- Bfb8d1f960d30680489806f209e8bb552 annotatedTarget "An autosomal recessive disorder caused by mutation(s) in the ADAT3 gene, encoding probable inactive tRNA-specific adenosine deaminase-like protein 3. It is characterized by a neurodevelopmental disorder with brain abnormalities, poor growth, and abnormal facies." @default.