Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf78b2b165f0dd8152f0b0b90b6024cc8> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bf78b2b165f0dd8152f0b0b90b6024cc8 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- Bf78b2b165f0dd8152f0b0b90b6024cc8 type Axiom @default.
- Bf78b2b165f0dd8152f0b0b90b6024cc8 annotatedProperty IAO_0000115 @default.
- Bf78b2b165f0dd8152f0b0b90b6024cc8 annotatedSource MONDO_0013551 @default.
- Bf78b2b165f0dd8152f0b0b90b6024cc8 annotatedTarget "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4B1 gene." @default.