INT192784

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Context Info
Confidence 0.45
First Reported 2006
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 2
Total Number 2
Disease Relevance 3.39
Pain Relevance 0.04

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

pigmentation (Myo5a) Golgi apparatus (Myo5a) cytoplasm (Myo5a)
Myo5a (Mus musculus)
Pain Link Frequency Relevance Heat
anakinra 2 75.64 Quite High
Inflammation 12 43.60 Quite Low
cINOD 3 5.00 Very Low Very Low Very Low
corticosteroid 1 5.00 Very Low Very Low Very Low
anesthesia 1 5.00 Very Low Very Low Very Low
Inflammatory response 1 5.00 Very Low Very Low Very Low
abdominal pain 1 5.00 Very Low Very Low Very Low
rheumatoid arthritis 1 5.00 Very Low Very Low Very Low
headache 1 5.00 Very Low Very Low Very Low
antagonist 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Mevalonate Kinase Deficiency 38 100.00 Very High Very High Very High
Syndrome 35 100.00 Very High Very High Very High
Pox Virus Infection 1 99.72 Very High Very High Very High
Respiratory Syncytial Virus 143 95.28 Very High Very High Very High
Disease 18 94.96 High High
Sprains And Strains 11 86.40 High High
Fever 21 83.20 Quite High
Ataxia 8 72.64 Quite High
Mucoepidermoid Carcinoma 2 72.52 Quite High
Dementia 4 71.12 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Modified vaccinia virus Ankara expressing T7 RNA polymerase (MVA-T7) was kindly provided by G.
Positive_regulation (provided) of Gene_expression (expressing) of MVA associated with pox virus infection
1) Confidence 0.45 Published 2010 Journal Virol J Section Body Doc Link PMC2887800 Disease Relevance 1.29 Pain Relevance 0
Mutations in the MVK gene and reduced activity of MVK have been identified as underlying cause of both MVA and HIDS syndrome.
Positive_regulation (cause) of Gene_expression (syndrome) of MVA associated with mevalonate kinase deficiency and syndrome
2) Confidence 0.03 Published 2006 Journal Orphanet J Rare Dis Section Body Doc Link PMC1475558 Disease Relevance 2.11 Pain Relevance 0.04

General Comments

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