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- NCIT_C186789 IAO_0000115 "An autosomal recessive disorder caused by mutation(s) in the ADAT3 gene, encoding probable inactive tRNA-specific adenosine deaminase-like protein 3. It is characterized by a neurodevelopmental disorder with brain abnormalities, poor growth, and abnormal facies." @default.
- NCIT_C186789 NCIT_NHC0 "C186789" @default.
- NCIT_C186789 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C186789 NCIT_P108 "Neurodevelopmental Disorder with Brain Abnormalities, Poor Growth, and Dysmorphic Facies" @default.
- NCIT_C186789 NCIT_P208 "CL941994" @default.
- NCIT_C186789 NCIT_P322 "Cellosaurus" @default.
- NCIT_C186789 NCIT_R176 NCIT_C16612 @default.
- NCIT_C186789 NCIT_R176 NCIT_C191897 @default.
- NCIT_C186789 NCIT_R176 NCIT_C20194 @default.
- NCIT_C186789 normalizedInformationContent "100" @default.
- NCIT_C186789 referenceCount "1" @default.
- NCIT_C186789 hasExactSynonym "Intellectual Disability-Strabismus Syndrome" @default.
- NCIT_C186789 hasExactSynonym "NEDBGF" @default.
- NCIT_C186789 hasExactSynonym "Neurodevelopmental Disorder with Brain Abnormalities, Poor Growth, and Dysmorphic Facies" @default.
- NCIT_C186789 inSubset NCIT_C165258 @default.
- NCIT_C186789 inSubset NCIT_C192842 @default.
- NCIT_C186789 type Class @default.
- NCIT_C186789 isDefinedBy ncit.owl @default.
- NCIT_C186789 label "Neurodevelopmental Disorder with Brain Abnormalities, Poor Growth, and Dysmorphic Facies" @default.
- NCIT_C186789 subClassOf B85766cfea3fd429c9bb7eaebffe93239 @default.
- NCIT_C186789 subClassOf Bb5c33521bae734a5e780ec1e066c89a7 @default.
- NCIT_C186789 subClassOf NCIT_C186789 @default.
- NCIT_C186789 subClassOf NCIT_C28193 @default.
- NCIT_C186789 subClassOf NCIT_C2991 @default.
- NCIT_C186789 subClassOf NCIT_C7057 @default.