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- NCIT_C168598 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the GRIN2A gene, encoding glutamate receptor ionotropic NMDA 2A. It is characterized by childhood-onset seizures affecting the temporal lobe or rolandic area of the brain, with a variable phenotype. It often affects speech and language." @default.
- NCIT_C168598 NCIT_NHC0 "C168598" @default.
- NCIT_C168598 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C168598 NCIT_P108 "Epilepsy, Focal, with Speech Disorder and with or without Mental Retardation" @default.
- NCIT_C168598 NCIT_P207 "C3806402" @default.
- NCIT_C168598 NCIT_P322 "Cellosaurus" @default.
- NCIT_C168598 NCIT_R176 NCIT_C16612 @default.
- NCIT_C168598 NCIT_R176 NCIT_C21295 @default.
- NCIT_C168598 NCIT_R176 NCIT_C25869 @default.
- NCIT_C168598 NCIT_R176 NCIT_C25993 @default.
- NCIT_C168598 NCIT_R176 NCIT_C26039 @default.
- NCIT_C168598 NCIT_R176 NCIT_C28533 @default.
- NCIT_C168598 NCIT_R176 NCIT_C98146 @default.
- NCIT_C168598 normalizedInformationContent "100" @default.
- NCIT_C168598 referenceCount "1" @default.
- NCIT_C168598 hasExactSynonym "Aphasia, Acquired, with Epilepsy" @default.
- NCIT_C168598 hasExactSynonym "Epilepsy, Focal, with Speech Disorder and with or without Mental Retardation" @default.
- NCIT_C168598 hasExactSynonym "FESD with or without Mental Retardation" @default.
- NCIT_C168598 inSubset NCIT_C165258 @default.
- NCIT_C168598 inSubset NCIT_C192842 @default.
- NCIT_C168598 type Class @default.
- NCIT_C168598 isDefinedBy ncit.owl @default.
- NCIT_C168598 label "Epilepsy, Focal, with Speech Disorder and with or without Mental Retardation" @default.
- NCIT_C168598 subClassOf B48cbe02b127ac7c4edcd7a57678c45d0 @default.
- NCIT_C168598 subClassOf Be387ad592ff4de753767d31945903dde @default.
- NCIT_C168598 subClassOf NCIT_C168598 @default.
- NCIT_C168598 subClassOf NCIT_C2991 @default.
- NCIT_C168598 subClassOf NCIT_C4873 @default.
- NCIT_C168598 subClassOf NCIT_C53529 @default.
- NCIT_C168598 subClassOf NCIT_C53543 @default.
- NCIT_C168598 subClassOf NCIT_C53547 @default.
- NCIT_C168598 subClassOf NCIT_C7057 @default.