Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bb3b6e5e89c4fdd4a7ddaf0b4a10c3061> ?p ?o ?g. }
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- Bb3b6e5e89c4fdd4a7ddaf0b4a10c3061 hasDbXref "NCIT:C131647" @default.
- Bb3b6e5e89c4fdd4a7ddaf0b4a10c3061 type Axiom @default.
- Bb3b6e5e89c4fdd4a7ddaf0b4a10c3061 annotatedProperty IAO_0000115 @default.
- Bb3b6e5e89c4fdd4a7ddaf0b4a10c3061 annotatedSource MONDO_0009865 @default.
- Bb3b6e5e89c4fdd4a7ddaf0b4a10c3061 annotatedTarget "A rare, autosomal recessive, inherited disorder caused by mutation of the PGAM2 gene. It is characterized by non-spherocytic hemolytic anemia, exercise-induced cramping, myoglobinuria, and presence of tubular aggregates on muscle biopsy." @default.