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- NCIT_C189277 IAO_0000115 "An autosomal dominant subtype of familial hemiplegic migraine caused by mutation(s) in the CACNA1A gene, encoding voltage-dependent P/Q-type calcium channel subunit alpha-1A." @default.
- NCIT_C189277 NCIT_NHC0 "C189277" @default.
- NCIT_C189277 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C189277 NCIT_P108 "Familial Hemiplegic Migraine-1" @default.
- NCIT_C189277 NCIT_P207 "C1832884" @default.
- NCIT_C189277 NCIT_P322 "Cellosaurus" @default.
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- NCIT_C189277 NCIT_R100 NCIT_C12755 @default.
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- NCIT_C189277 NCIT_R176 NCIT_C16612 @default.
- NCIT_C189277 NCIT_R176 NCIT_C191380 @default.
- NCIT_C189277 NCIT_R176 NCIT_C21295 @default.
- NCIT_C189277 NCIT_R176 NCIT_C25869 @default.
- NCIT_C189277 NCIT_R176 NCIT_C25993 @default.
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- NCIT_C189277 NCIT_R176 NCIT_C28533 @default.
- NCIT_C189277 normalizedInformationContent "100" @default.
- NCIT_C189277 referenceCount "1" @default.
- NCIT_C189277 hasExactSynonym "FHM1" @default.
- NCIT_C189277 hasExactSynonym "Familial Hemiplegic Migraine-1" @default.
- NCIT_C189277 inSubset NCIT_C165258 @default.
- NCIT_C189277 inSubset NCIT_C192842 @default.
- NCIT_C189277 type Class @default.
- NCIT_C189277 isDefinedBy ncit.owl @default.
- NCIT_C189277 label "Familial Hemiplegic Migraine-1" @default.
- NCIT_C189277 subClassOf B659d2a8b23ddbc58c9e5a478849c839d @default.
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- NCIT_C189277 subClassOf NCIT_C189277 @default.
- NCIT_C189277 subClassOf NCIT_C26835 @default.
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- NCIT_C189277 subClassOf NCIT_C89715 @default.