INT265514

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Context Info
Confidence 0.42
First Reported 2009
Last Reported 2009
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.82
Pain Relevance 0

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

transport (COX1) mitochondrion (COX1) oxidoreductase activity (COX1)
COX1 (Mus musculus)
Pain Link Frequency Relevance Heat
Inflammation 2 5.00 Very Low Very Low Very Low
Pain 2 5.00 Very Low Very Low Very Low
cva 2 5.00 Very Low Very Low Very Low
imagery 1 5.00 Very Low Very Low Very Low
alcohol 1 5.00 Very Low Very Low Very Low
headache 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Cytochrome-c Oxidase Deficiency 1 100.00 Very High Very High Very High
Atrophy 7 94.72 High High
Inborn Genetic Diseases 1 87.48 High High
Optic Atrophy 6 75.12 Quite High
Disease 11 72.20 Quite High
Leber Hereditary Optic Atrophy 4 68.04 Quite High
Toxicity 1 51.44 Quite High
Optic Disorders 8 42.00 Quite Low
Deafness 2 22.68 Low Low
Pressure And Volume Under Development 5 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The novel OPA1 mutation is associated with a mitochondrial energy defect involving reduced ATP synthesis and a cytochrome c oxidase deficiency.
Negative_regulation (deficiency) of cytochrome c oxidase associated with cytochrome-c oxidase deficiency
1) Confidence 0.42 Published 2009 Journal Molecular Vision Section Body Doc Link PMC2661005 Disease Relevance 0.82 Pain Relevance 0

General Comments

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