Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C132292> ?p ?o ?g. }
Showing items 1 to 30 of
30
with 100 items per page.
- NCIT_C132292 IAO_0000115 "Congenital myasthenic syndrome caused by mutation(s) in the CHAT gene, encoding choline O-acetyltransferase. It is inherited in an autosomal recessive manner." @default.
- NCIT_C132292 NCIT_NHC0 "C132292" @default.
- NCIT_C132292 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C132292 NCIT_P108 "Presynaptic Congenital Myasthenic Syndrome 6" @default.
- NCIT_C132292 NCIT_P207 "C0393929" @default.
- NCIT_C132292 NCIT_P322 "Cellosaurus" @default.
- NCIT_C132292 NCIT_R176 NCIT_C104885 @default.
- NCIT_C132292 NCIT_R176 NCIT_C16612 @default.
- NCIT_C132292 NCIT_R176 NCIT_C21281 @default.
- NCIT_C132292 NCIT_R176 NCIT_C25870 @default.
- NCIT_C132292 normalizedInformationContent "100" @default.
- NCIT_C132292 referenceCount "1" @default.
- NCIT_C132292 hasExactSynonym "CMS6" @default.
- NCIT_C132292 hasExactSynonym "Presynaptic Congenital Myasthenic Syndrome 6" @default.
- NCIT_C132292 inSubset NCIT_C165258 @default.
- NCIT_C132292 inSubset NCIT_C192842 @default.
- NCIT_C132292 type Class @default.
- NCIT_C132292 isDefinedBy ncit.owl @default.
- NCIT_C132292 label "Presynaptic Congenital Myasthenic Syndrome 6" @default.
- NCIT_C132292 subClassOf Bc5393f5847774ade61de05541f785cfd @default.
- NCIT_C132292 subClassOf Be1bc7f3bda7d5e41395a8a0d79ff41ca @default.
- NCIT_C132292 subClassOf NCIT_C132292 @default.
- NCIT_C132292 subClassOf NCIT_C28193 @default.
- NCIT_C132292 subClassOf NCIT_C2991 @default.
- NCIT_C132292 subClassOf NCIT_C4873 @default.
- NCIT_C132292 subClassOf NCIT_C53529 @default.
- NCIT_C132292 subClassOf NCIT_C53543 @default.
- NCIT_C132292 subClassOf NCIT_C53547 @default.
- NCIT_C132292 subClassOf NCIT_C7057 @default.
- NCIT_C132292 subClassOf NCIT_C84647 @default.