Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B4422341d7ef45826911301cca694b5f5> ?p ?o ?g. }
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- B4422341d7ef45826911301cca694b5f5 NCIT_P378 "NCI" @default.
- B4422341d7ef45826911301cca694b5f5 type Axiom @default.
- B4422341d7ef45826911301cca694b5f5 annotatedProperty IAO_0000115 @default.
- B4422341d7ef45826911301cca694b5f5 annotatedSource NCIT_C181657 @default.
- B4422341d7ef45826911301cca694b5f5 annotatedTarget "An autosomal recessive subtype of hereditary spastic paraplegia caused by mutation(s) in the SPG7 gene, encoding paraplegin." @default.