INT331971

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Context Info
Confidence 0.31
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.00
Pain Relevance 0.13

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

enzyme binding (DNM2) GTPase activity (DNM2) cytoplasm (DNM2)
cytosol (DNM2) signal transduction (DNM2) nucleus (DNM2)
Anatomy Link Frequency
muscle 2
DNM2 (Homo sapiens)
Pain Link Frequency Relevance Heat
imagery 120 99.32 Very High Very High Very High
Inflammation 10 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Channelopathies 5 99.12 Very High Very High Very High
Muscle Disease 51 97.92 Very High Very High Very High
Hypopituitarism 3 68.80 Quite High
Pressure And Volume Under Development 5 51.36 Quite High
Nemaline Myopathy 1 34.12 Quite Low
Disease 23 24.40 Low Low
Congenital Structural Myopathies 2 12.56 Low Low
Muscular Dystrophy 37 5.00 Very Low Very Low Very Low
Frailty 12 5.00 Very Low Very Low Very Low
INFLAMMATION 8 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Typical muscle imaging findings of patients with proven mutations in the DNM2, SEPN1, ACTA1, RYR1 and collagen 6A1 are provided

Muscle channelopathies and metabolic myopathies

Positive_regulation (mutations) of Gene_expression (6A1) of DNM2 in muscle associated with muscle disease, channelopathies and imagery
1) Confidence 0.31 Published 2010 Journal Eur Radiol Section Body Doc Link PMC2940021 Disease Relevance 1.00 Pain Relevance 0.13

General Comments

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