Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B61b8b0c55915d3578b60228b8ecbe00b> ?p ?o ?g. }
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- B61b8b0c55915d3578b60228b8ecbe00b hasDbXref 0000-0002-1735-8178 @default.
- B61b8b0c55915d3578b60228b8ecbe00b type Axiom @default.
- B61b8b0c55915d3578b60228b8ecbe00b annotatedProperty IAO_0000115 @default.
- B61b8b0c55915d3578b60228b8ecbe00b annotatedSource HP_0033725 @default.
- B61b8b0c55915d3578b60228b8ecbe00b annotatedTarget "An abnormally thin corpus callous, due to atrophy, hypoplasia or agenesis. This term is intended to be used in situations where it is not known if thinning of the corpus callosum (for instance, as visualized by magnetic resonance tomography) is due to abnormal development (e.g. a leukodystrophy) or atrophy following normal development (e.g. neurodegeneration)." @default.