INT345139

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Context Info
Confidence 0.01
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.53
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.

Anatomy Link Frequency
hair 1
Rhs1 (Mus musculus)
Pain Link Frequency Relevance Heat
antagonist 15 76.08 Quite High
Neuropathic pain 8 7.68 Low Low
agonist 15 5.00 Very Low Very Low Very Low
fibrosis 9 5.00 Very Low Very Low Very Low
dorsal root ganglion 4 5.00 Very Low Very Low Very Low
Pain 4 5.00 Very Low Very Low Very Low
metalloproteinase 4 5.00 Very Low Very Low Very Low
Potency 3 5.00 Very Low Very Low Very Low
alcohol 2 5.00 Very Low Very Low Very Low
Multiple sclerosis 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Hypotrichosis 3 100.00 Very High Very High Very High
Carcinoma 1 92.44 High High
Disease 7 92.32 High High
Adenocarcinoma 1 91.32 High High
Skin Cancer 3 90.44 High High
Syndrome 1 45.76 Quite Low
Neuropathic Pain 10 7.68 Low Low
Cancer 24 5.00 Very Low Very Low Very Low
Ovarian Cancer 16 5.00 Very Low Very Low Very Low
Targeted Disruption 15 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
An unbiased genetic search for the gene causing familial Hypotrichosis simplex and autosomal recessive woolly hair has identified mutations in the P2Y5 receptor gene on chromosome 13q14.2–14.3 (Z = 17.97) (Pasternack et al., 2008; Shimomura et al., 2008) underlying the disease.
Positive_regulation (causing) of Hypotrichosis simplex in hair associated with hypotrichosis and disease
1) Confidence 0.01 Published 2010 Journal British Journal of Pharmacology Section Body Doc Link PMC2989581 Disease Relevance 0.53 Pain Relevance 0.04

General Comments

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