INT274203

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Context Info
Confidence 0.16
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 2.41
Pain Relevance 0.37

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

nucleoplasm (PABPN1) mRNA processing (PABPN1) nucleolus (PABPN1)
RNA binding (PABPN1) nucleus (PABPN1) cytoplasm (PABPN1)
PABPN1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Pain 7 87.60 High High
corticosteroid 8 86.60 High High
Inflammation 15 81.80 Quite High
fifth nerve 1 71.72 Quite High
fibrosis 6 32.56 Quite Low
imagery 8 5.00 Very Low Very Low Very Low
cytokine 2 5.00 Very Low Very Low Very Low
headache 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Oculopharyngeal Muscular Dystrophy 4 100.00 Very High Very High Very High
Dysphagia 1 93.28 High High
Ophthalmoplegia 8 92.84 High High
Ocular Toxicity (including Many Sub-types) 11 90.64 High High
Syndrome 17 88.12 High High
Pain 3 87.60 High High
Spontaneous Remission 1 85.52 High High
Frailty 5 82.24 Quite High
Granulomatous Inflammation 1 81.80 Quite High
INFLAMMATION 13 80.20 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
OPMD is caused by expansions in a 6 GCG trinucleotide repeat tract located in the first exon of the polyadenylate binding protein nuclear 1 gene on chromosome 14q (Brais 2003; Ruegg et al 2005).
Positive_regulation (caused) of OPMD associated with oculopharyngeal muscular dystrophy
1) Confidence 0.16 Published 2007 Journal Clinical ophthalmology (Auckland, N.Z.) Section Body Doc Link PMC2699981 Disease Relevance 2.41 Pain Relevance 0.37

General Comments

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