Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B6f26b2406abf73d55d9bce74d0a3679d> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B6f26b2406abf73d55d9bce74d0a3679d hasDbXref "NCIT:C125695" @default.
- B6f26b2406abf73d55d9bce74d0a3679d type Axiom @default.
- B6f26b2406abf73d55d9bce74d0a3679d annotatedProperty IAO_0000115 @default.
- B6f26b2406abf73d55d9bce74d0a3679d annotatedSource MONDO_0003122 @default.
- B6f26b2406abf73d55d9bce74d0a3679d annotatedTarget "A progressive neurodegenerative disorder caused by a disruption in the connection between the striatum and the substantia nigra. It is a type of multiple system atrophy (MSA). Signs and symptoms include rigidity, instability, impaired speech, and slow movements." @default.