INT289626

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Context Info
Confidence 0.03
First Reported 2009
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 3
Total Number 3
Disease Relevance 2.49
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.

cytosol (SUGT1) nucleoplasm (SNRNP70) mitosis (SUGT1)
mRNA processing (SNRNP70) RNA binding (SNRNP70) nucleus (SNRNP70)
SNRNP70 (Homo sapiens)
SUGT1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Multiple sclerosis 96 47.32 Quite Low
rheumatoid arthritis 100 42.48 Quite Low
Arthritis 14 21.32 Low Low
spinal inflammation 50 5.00 Very Low Very Low Very Low
Crohn's disease 26 5.00 Very Low Very Low Very Low
Inflammation 10 5.00 Very Low Very Low Very Low
psoriasis 6 5.00 Very Low Very Low Very Low
Central nervous system 2 5.00 Very Low Very Low Very Low
Angina 2 5.00 Very Low Very Low Very Low
Infliximab 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Diabetes Mellitus 135 100.00 Very High Very High Very High
Disease 304 99.04 Very High Very High Very High
Coronary Artery Disease 39 98.70 Very High Very High Very High
Myocardial Infarction 36 85.40 High High
Autoimmune Disease 106 50.00 Quite Low
Demyelinating Disease 100 47.32 Quite Low
Rheumatoid Arthritis 114 42.48 Quite Low
Thyroid Disease 68 5.00 Very Low Very Low Very Low
Low Back Pain 50 5.00 Very Low Very Low Very Low
Hypertension 13 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
SNP rs2891168 was confirmed as associated with CAD (p < 0.0001) with a G-allele OR of 1.28 (95% CI 1.20-1.36), and SNP rs10811661 was associated with T2D (p = 0.04) with a T-allele OR of 1.19 (95%CI 1.01-1.41).
SNP Binding (associated) of T-allele OR associated with coronary artery disease and diabetes mellitus
1) Confidence 0.03 Published 2010 Journal BMC Med Genet Section Body Doc Link PMC2871267 Disease Relevance 1.84 Pain Relevance 0
We define the notion of a genetic variation profile as a combination of log-odds scores and p-values for each SNP measuring allele-specific association between the SNP and each of the eleven diseases in the combined dataset.
SNP Binding (association) of allele associated with disease
2) Confidence 0.00 Published 2009 Journal PLoS Genetics Section Body Doc Link PMC2791168 Disease Relevance 0.33 Pain Relevance 0
We define the notion of a genetic variation profile as a combination of log-odds scores and p-values for each SNP measuring allele-specific association between the SNP and each of the eleven diseases in the combined dataset.
SNP Binding (association) of allele associated with disease
3) Confidence 0.00 Published 2009 Journal PLoS Genetics Section Body Doc Link PMC2791168 Disease Relevance 0.33 Pain Relevance 0

General Comments

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