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- NCIT_C147531 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the SCN9A gene, encoding sodium channel protein type 9 subunit alpha. It is characterized by episodes of recurrent warmth, redness, and burning sensations in the extremities." @default.
- NCIT_C147531 NCIT_NHC0 "C147531" @default.
- NCIT_C147531 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C147531 NCIT_P108 "Primary Erythermalgia" @default.
- NCIT_C147531 NCIT_P310 "Retired_Concept" @default.
- NCIT_C147531 NCIT_P98 "Wed May 30 12:58:26 EDT 2018 - See 'Primary Erythromelalgia(C125383)'" @default.
- NCIT_C147531 normalizedInformationContent "100" @default.
- NCIT_C147531 referenceCount "1" @default.
- NCIT_C147531 hasExactSynonym "PERYTHM" @default.
- NCIT_C147531 hasExactSynonym "Primary Erythermalgia" @default.
- NCIT_C147531 hasExactSynonym "Primary Erythromelalgia" @default.
- NCIT_C147531 type Class @default.
- NCIT_C147531 isDefinedBy ncit.owl @default.
- NCIT_C147531 label "Primary Erythermalgia" @default.
- NCIT_C147531 subClassOf NCIT_C147531 @default.
- NCIT_C147531 subClassOf NCIT_C157491 @default.
- NCIT_C147531 subClassOf NCIT_C28428 @default.
- NCIT_C147531 deprecated "true" @default.