Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bdd4e69f3b55b9a0af6b9e7251912d4e8> ?p ?o ?g. }
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- Bdd4e69f3b55b9a0af6b9e7251912d4e8 hasDbXref "PMID:33230297" @default.
- Bdd4e69f3b55b9a0af6b9e7251912d4e8 hasDbXref "https://orcid.org/0000-0002-7371-8158" @default.
- Bdd4e69f3b55b9a0af6b9e7251912d4e8 hasDbXref "https://orcid.org/0000-0003-0113-912X" @default.
- Bdd4e69f3b55b9a0af6b9e7251912d4e8 type Axiom @default.
- Bdd4e69f3b55b9a0af6b9e7251912d4e8 annotatedProperty IAO_0000115 @default.
- Bdd4e69f3b55b9a0af6b9e7251912d4e8 annotatedSource MONDO_0030361 @default.
- Bdd4e69f3b55b9a0af6b9e7251912d4e8 annotatedTarget "A type I interferonopathy characterized by severe developmental delay and progressive neurologic deterioration ending in premature death. Brain imaging shows diffusely abnormal white matter, severe cerebral atrophy, and intracranial calcification." @default.