INT142994

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Context Info
Confidence 0.00
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Title
Documents 1
Total Number 1
Disease Relevance 0.91
Pain Relevance 0.70

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

cytosol (UPF1) RNA binding (UPF1) helicase activity (UPF1)
cell cycle (UPF1) DNA binding (UPF1) cytoplasm (UPF1)
UPF1 (Homo sapiens)
FCMTE1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Migraine 7 98.96 Very High Very High Very High
sodium channel 2 85.48 High High
Disease Link Frequency Relevance Heat
Epilepsy 2 100.00 Very High Very High Very High
Migraine With Aura 6 99.76 Very High Very High Very High
Headache 1 93.68 High High
Paresis 1 93.12 High High
Ataxia 1 81.92 Quite High
Brain Disease 1 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies.
mutation Binding (associated) of SCN1A epilepsy gene associated with epilepsy, migraine with aura and migraine
1) Confidence 0.00 Published 2007 Journal Hum. Mutat. Section Title Doc Link 17397047 Disease Relevance 0.91 Pain Relevance 0.70

General Comments

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