INT328872

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Context Info
Confidence 0.00
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 1
Disease Relevance 1.30
Pain Relevance 0.17

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

nucleus (ZNF434) intracellular (ZNF434) DNA binding (ZNF434)
ZNF434 (Homo sapiens)
Pain Link Frequency Relevance Heat
COX2 3 100.00 Very High Very High Very High
Inflammation 32 91.84 High High
Inflammatory response 6 5.00 Very Low Very Low Very Low
cytokine 3 5.00 Very Low Very Low Very Low
fibrosis 1 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Esophageal Disease 36 98.90 Very High Very High Very High
Disease 2 94.68 High High
Non-small-cell Lung Cancer 8 92.92 High High
INFLAMMATION 38 91.84 High High
Pneumonia 36 88.72 High High
Toxicity 20 85.60 High High
Lung Cancer 4 77.68 Quite High
Nicotine Addiction 8 5.00 Very Low Very Low Very Low
Cancer 7 5.00 Very Low Very Low Very Low
Immunotherapy Of Cancer 2 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
For esophagitis risk, nine SNPs were associated with a 1.5- to 4-fold increase in risk, including three PTGS2 (COX2) variants: rs20417 (HR:1.93, 95% CI:1.10–3.39), rs5275 (HR:1.58, 95% CI:1.09–2.27), and rs689470 (HR:3.38, 95% CI:1.09–10.49).
Positive_regulation (increase) of rs20417 associated with esophageal disease and cox2
1) Confidence 0.00 Published 2010 Journal PLoS ONE Section Abstract Doc Link PMC2928273 Disease Relevance 1.30 Pain Relevance 0.17

General Comments

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