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- NCIT_C179708 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the DYRK1A gene, encoding dual specificity tyrosine-phosphorylation-regulated kinase 1A. It is characterized by moderate-severe intellectual disability and typical facial dysmorphisms." @default.
- NCIT_C179708 NCIT_NHC0 "C179708" @default.
- NCIT_C179708 NCIT_P106 "Mental or Behavioral Dysfunction" @default.
- NCIT_C179708 NCIT_P108 "Mental Retardation, Autosomal Dominant 7" @default.
- NCIT_C179708 NCIT_P207 "C3279839" @default.
- NCIT_C179708 NCIT_P322 "Cellosaurus" @default.
- NCIT_C179708 NCIT_R176 NCIT_C16612 @default.
- NCIT_C179708 NCIT_R176 NCIT_C21281 @default.
- NCIT_C179708 NCIT_R176 NCIT_C25870 @default.
- NCIT_C179708 NCIT_R176 NCIT_C25871 @default.
- NCIT_C179708 NCIT_R176 NCIT_C25872 @default.
- NCIT_C179708 NCIT_R176 NCIT_C98170 @default.
- NCIT_C179708 normalizedInformationContent "100" @default.
- NCIT_C179708 referenceCount "1" @default.
- NCIT_C179708 hasExactSynonym "MRD7" @default.
- NCIT_C179708 hasExactSynonym "Mental Retardation, Autosomal Dominant 7" @default.
- NCIT_C179708 inSubset NCIT_C165258 @default.
- NCIT_C179708 inSubset NCIT_C192842 @default.
- NCIT_C179708 type Class @default.
- NCIT_C179708 isDefinedBy ncit.owl @default.
- NCIT_C179708 label "Mental Retardation, Autosomal Dominant 7" @default.
- NCIT_C179708 subClassOf B4df0fe94fda5762add6290b37d3950b3 @default.
- NCIT_C179708 subClassOf B74ec506f65f58305e496b35859cf5391 @default.
- NCIT_C179708 subClassOf NCIT_C179708 @default.
- NCIT_C179708 subClassOf NCIT_C2991 @default.
- NCIT_C179708 subClassOf NCIT_C7057 @default.
- NCIT_C179708 subClassOf NCIT_C84392 @default.
- NCIT_C179708 subClassOf NCIT_C89328 @default.
- NCIT_C179708 subClassOf NCIT_C89330 @default.