Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8f8909eca7510686d8f1d205a1df849e> ?p ?o ?g. }
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- B8f8909eca7510686d8f1d205a1df849e hasDbXref "PMID:29193663" @default.
- B8f8909eca7510686d8f1d205a1df849e hasDbXref "PMID:29430868" @default.
- B8f8909eca7510686d8f1d205a1df849e hasDbXref "PMID:30543385" @default.
- B8f8909eca7510686d8f1d205a1df849e hasDbXref "PMID:321171285" @default.
- B8f8909eca7510686d8f1d205a1df849e hasDbXref "https://www.clinicalgenome.org/affiliation/40006/" @default.
- B8f8909eca7510686d8f1d205a1df849e type Axiom @default.
- B8f8909eca7510686d8f1d205a1df849e annotatedProperty IAO_0000115 @default.
- B8f8909eca7510686d8f1d205a1df849e annotatedSource MONDO_0017241 @default.
- B8f8909eca7510686d8f1d205a1df849e annotatedTarget "A disorder that presents with spastic paraplegia and intellectual disability in which the cause of the disease is a mutation in the AP4B1 gene." @default.