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The way concept relations are shown:
Neurofibromin 1
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ Neurofibromin 1 16 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Neurofibromin 1 16 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Neurofibromin 1 16 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Neurofibromin 1 16 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
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historyNote*: | 2002
X |
publicMeSHNote*: | 2002
X |
Scope note: | A protein found most abundantly in the nervous system. Defects or deficiencies in this protein are associated with NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome. Mutations in the gene (GENE, NEUROFIBROMATOSIS 1) affect two known functions: regulation of ras-GTPase and tumor suppression.
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activeMeSHYear*: | |
dateCreated*: | 2001-07-25X |
dateEstablished*: | 2002-01-01X |
dateRevised*: | 2004-07-29X |
recordAuthorizer*: | jlsX |
recordMaintainer*: | jlsX |
recordOriginator*: | nnsX |
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Labels and equivalent concepts: | Neurofibromiini 1 (fi) XNF1 Protein (en, replaced) NF1-GAP-Related Protein (en, replaced) NF1 GRP (en, replaced) NF-1 Protein (en, replaced) Neurofibromatosis Type 1 Gene Product (en, replaced) Neurofibromatosis Type 1 Protein (en, replaced) Neurofibromin (en, replaced) Neurofibromina 1 (es) Proteína Tipo 1 de Neurofibromatosis (es, replaced) Neurofibromatose-Typ-1-Protein (de, replaced) |
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