Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5b3ba6eff2bbf3467d9faae6e099b95e> ?p ?o ?g. }
Showing items 1 to 7 of
7
with 100 items per page.
- B5b3ba6eff2bbf3467d9faae6e099b95e hasDbXref "OMIM:619423" @default.
- B5b3ba6eff2bbf3467d9faae6e099b95e hasDbXref "https://orcid.org/0000-0002-7371-8158" @default.
- B5b3ba6eff2bbf3467d9faae6e099b95e hasDbXref "https://orcid.org/0000-0003-0113-912X" @default.
- B5b3ba6eff2bbf3467d9faae6e099b95e type Axiom @default.
- B5b3ba6eff2bbf3467d9faae6e099b95e annotatedProperty IAO_0000115 @default.
- B5b3ba6eff2bbf3467d9faae6e099b95e annotatedSource MONDO_0030378 @default.
- B5b3ba6eff2bbf3467d9faae6e099b95e annotatedTarget "An autosomal recessive disorder characterized by hypomyelination, microcephaly, liver dysfunction, and recurrent hypomyelination." @default.