INT111380

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Context Info
Confidence 0.03
First Reported 2003
Last Reported 2003
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 2
Disease Relevance 0.92
Pain Relevance 0.19

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

plasma membrane (Musk, Phka2) kinase activity (Musk, Phka2) signal transduction (Musk)
carbohydrate metabolic process (Phka2)
Anatomy Link Frequency
Muscle 2
Musk (Mus musculus)
Phka2 (Mus musculus)
Pain Link Frequency Relevance Heat
Pain 2 95.68 Very High Very High Very High
Disease Link Frequency Relevance Heat
Glycogen Storage Disease 8 99.64 Very High Very High Very High
Pain 2 95.68 Very High Very High Very High
Cramps 2 95.44 Very High Very High Very High
Myoglobinuria 2 94.48 High High
Congenital Anomalies 2 25.00 Low Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Muscle-specific deficiency of phosphorylase kinase (Phk) causes glycogen storage disease, clinically manifesting in exercise intolerance with early fatiguability, pain, cramps and occasionally myoglobinuria.
Muscle-specific Negative_regulation (deficiency) of phosphorylase kinase in Muscle associated with cramps, pain, myoglobinuria and glycogen storage disease
1) Confidence 0.03 Published 2003 Journal Eur. J. Hum. Genet. Section Abstract Doc Link 12825073 Disease Relevance 0.46 Pain Relevance 0.10
Muscle-specific deficiency of phosphorylase kinase (Phk) causes glycogen storage disease, clinically manifesting in exercise intolerance with early fatiguability, pain, cramps and occasionally myoglobinuria.
Muscle-specific Negative_regulation (deficiency) of Phk in Muscle associated with cramps, pain, myoglobinuria and glycogen storage disease
2) Confidence 0.03 Published 2003 Journal Eur. J. Hum. Genet. Section Abstract Doc Link 12825073 Disease Relevance 0.46 Pain Relevance 0.10

General Comments

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