Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C156309> ?p ?o ?g. }
Showing items 1 to 31 of
31
with 100 items per page.
- NCIT_C156309 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the MYT1L gene, encoding myelin transcription factor 1-like protein. It is characterized by intellectual disability and mild dysmorphic facial features." @default.
- NCIT_C156309 NCIT_NHC0 "C156309" @default.
- NCIT_C156309 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C156309 NCIT_P108 "Mental Retardation, Autosomal Dominant 39" @default.
- NCIT_C156309 NCIT_P207 "C4225296" @default.
- NCIT_C156309 NCIT_P322 "Cellosaurus" @default.
- NCIT_C156309 NCIT_R176 NCIT_C16612 @default.
- NCIT_C156309 NCIT_R176 NCIT_C20420 @default.
- NCIT_C156309 NCIT_R176 NCIT_C54362 @default.
- NCIT_C156309 NCIT_R176 NCIT_C82897 @default.
- NCIT_C156309 normalizedInformationContent "100" @default.
- NCIT_C156309 referenceCount "1" @default.
- NCIT_C156309 hasExactSynonym "MRD39" @default.
- NCIT_C156309 hasExactSynonym "Mental Retardation, Autosomal Dominant 39" @default.
- NCIT_C156309 inSubset NCIT_C165258 @default.
- NCIT_C156309 inSubset NCIT_C192842 @default.
- NCIT_C156309 type Class @default.
- NCIT_C156309 isDefinedBy ncit.owl @default.
- NCIT_C156309 label "Mental Retardation, Autosomal Dominant 39" @default.
- NCIT_C156309 subClassOf B1b3b0a15c26a7f5635136ff6fe9d27bf @default.
- NCIT_C156309 subClassOf B803a35230025475b361ee2d5cc7acdbf @default.
- NCIT_C156309 subClassOf NCIT_C156309 @default.
- NCIT_C156309 subClassOf NCIT_C2991 @default.
- NCIT_C156309 subClassOf NCIT_C4873 @default.
- NCIT_C156309 subClassOf NCIT_C53529 @default.
- NCIT_C156309 subClassOf NCIT_C53543 @default.
- NCIT_C156309 subClassOf NCIT_C53547 @default.
- NCIT_C156309 subClassOf NCIT_C7057 @default.
- NCIT_C156309 subClassOf NCIT_C84392 @default.
- NCIT_C156309 subClassOf NCIT_C89328 @default.
- NCIT_C156309 subClassOf NCIT_C89330 @default.