Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Be659ed8be87d47bf21c3198ce8e61843> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Be659ed8be87d47bf21c3198ce8e61843 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- Be659ed8be87d47bf21c3198ce8e61843 type Axiom @default.
- Be659ed8be87d47bf21c3198ce8e61843 annotatedProperty IAO_0000115 @default.
- Be659ed8be87d47bf21c3198ce8e61843 annotatedSource MONDO_0014360 @default.
- Be659ed8be87d47bf21c3198ce8e61843 annotatedTarget "Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the NECAP1 gene." @default.