Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B77fb87e33ee572dcff0ece1cb833a119> ?p ?o ?g. }
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- B77fb87e33ee572dcff0ece1cb833a119 hasDbXref "DOID:0110635" @default.
- B77fb87e33ee572dcff0ece1cb833a119 hasDbXref "PMID:11592034" @default.
- B77fb87e33ee572dcff0ece1cb833a119 hasDbXref "PMID:14652796" @default.
- B77fb87e33ee572dcff0ece1cb833a119 type Axiom @default.
- B77fb87e33ee572dcff0ece1cb833a119 annotatedProperty IAO_0000115 @default.
- B77fb87e33ee572dcff0ece1cb833a119 annotatedSource MONDO_0011688 @default.
- B77fb87e33ee572dcff0ece1cb833a119 annotatedTarget "A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with variable penetrance of intellectual disability and structural brain abnormalities that has material basis in homozygous or compound heterozygous mutation in the FKRP gene on chromosome 19q13.3." @default.