INT61991

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Context Info
Confidence 0.59
First Reported 1996
Last Reported 1996
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 1
Disease Relevance 1.67
Pain Relevance 0.08

This is a graph with borders and nodes. Maybe there is an Imagemap used so the nodes may be linking to some Pages.

pigmentation (NF1) signal transduction (NF1) nucleus (NF1)
intracellular (NF1) extracellular matrix organization (NF1) cytoplasm (NF1)
NF1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Pain 1 81.92 Quite High
Disease Link Frequency Relevance Heat
Watson Syndrome 7 100.00 Very High Very High Very High
Neurofibroma 3 99.54 Very High Very High Very High
Infarction 1 97.60 Very High Very High Very High
Cancer 3 97.16 Very High Very High Very High
Hyperplasia 1 95.12 Very High Very High Very High
Neurofibrosarcoma 2 89.40 High High
Pain 1 81.92 Quite High
Malignant Neoplastic Disease 1 76.20 Quite High
Plexiform Neurofibroma 1 75.56 Quite High
Syndrome 1 64.44 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The molecular basis of neurofibroma development in NF1 is loss of expression of the NF1 gene and its gene product, neurofibromin, resulting in elevated levels of Ras-guanosine triphosphate.
Negative_regulation (loss) of Gene_expression (expression) of NF1 associated with watson syndrome and neurofibroma
1) Confidence 0.59 Published 1996 Journal J. Neurosurg. Section Abstract Doc Link 8622163 Disease Relevance 1.67 Pain Relevance 0.08

General Comments

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