Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf0263fd2bf54f4ea4eaf2224dbaea4fc> ?p ?o ?g. }
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- Bf0263fd2bf54f4ea4eaf2224dbaea4fc hasDbXref "DOID:0112227" @default.
- Bf0263fd2bf54f4ea4eaf2224dbaea4fc hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- Bf0263fd2bf54f4ea4eaf2224dbaea4fc hasDbXref "https://clinicalgenome.org/affiliation/40006/" @default.
- Bf0263fd2bf54f4ea4eaf2224dbaea4fc type Axiom @default.
- Bf0263fd2bf54f4ea4eaf2224dbaea4fc annotatedProperty IAO_0000115 @default.
- Bf0263fd2bf54f4ea4eaf2224dbaea4fc annotatedSource MONDO_0100153 @default.
- Bf0263fd2bf54f4ea4eaf2224dbaea4fc annotatedTarget "A nervous system disorder characterized by complex cortical malformations including in most cases dysmorphic basal ganglia and/or corpus callosum in which the cause of the disease is a variation in a tubulin gene." @default.