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- NCIT_C168752 IAO_0000115 "An autosomal dominant form of amyotrophic lateral sclerosis caused by mutation(s) in the TARDBP gene, encoding TAR DNA-binding protein 43." @default.
- NCIT_C168752 NCIT_NHC0 "C168752" @default.
- NCIT_C168752 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C168752 NCIT_P108 "Amyotrophic Lateral Sclerosis 10, With or Without Frontotemporal Dementia" @default.
- NCIT_C168752 NCIT_P207 "C2677565" @default.
- NCIT_C168752 NCIT_P322 "Cellosaurus" @default.
- NCIT_C168752 NCIT_R100 NCIT_C12219 @default.
- NCIT_C168752 NCIT_R100 NCIT_C12438 @default.
- NCIT_C168752 NCIT_R100 NCIT_C12755 @default.
- NCIT_C168752 NCIT_R100 NCIT_C12919 @default.
- NCIT_C168752 NCIT_R100 NCIT_C13040 @default.
- NCIT_C168752 NCIT_R100 NCIT_C32221 @default.
- NCIT_C168752 NCIT_R176 NCIT_C16612 @default.
- NCIT_C168752 NCIT_R176 NCIT_C54362 @default.
- NCIT_C168752 NCIT_R176 NCIT_C80020 @default.
- NCIT_C168752 normalizedInformationContent "100" @default.
- NCIT_C168752 referenceCount "1" @default.
- NCIT_C168752 hasExactSynonym "ALS10" @default.
- NCIT_C168752 hasExactSynonym "Amyotrophic Lateral Sclerosis 10, With or Without Frontotemporal Dementia" @default.
- NCIT_C168752 inSubset NCIT_C165258 @default.
- NCIT_C168752 inSubset NCIT_C192842 @default.
- NCIT_C168752 type Class @default.
- NCIT_C168752 isDefinedBy ncit.owl @default.
- NCIT_C168752 label "Amyotrophic Lateral Sclerosis 10, With or Without Frontotemporal Dementia" @default.
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- NCIT_C168752 subClassOf NCIT_C4802 @default.
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- NCIT_C168752 subClassOf NCIT_C7057 @default.