INT132443

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Context Info
Confidence 0.44
First Reported 2006
Last Reported 2006
Negated 0
Speculated 0
Reported most in Title
Documents 1
Total Number 1
Disease Relevance 1.19
Pain Relevance 0.50

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

peptidase activity (MEP1A) extracellular space (MEP1A) cilium (EFHC1)
Anatomy Link Frequency
juvenile 1
MEP1A (Homo sapiens)
EFHC1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Migraine 7 100.00 Very High Very High Very High
Disease Link Frequency Relevance Heat
Headache 7 100.00 Very High Very High Very High
Juvenile Myoclonic Epilepsy 2 99.88 Very High Very High Very High
Epilepsy 2 89.20 High High
Disease 5 79.72 Quite High
Genetic Predisposition To Disease 1 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG.
MEP1A Binding (association) of EFHC1 in juvenile associated with juvenile myoclonic epilepsy and migraine
1) Confidence 0.44 Published 2006 Journal Neurosci. Lett. Section Title Doc Link 16378686 Disease Relevance 1.19 Pain Relevance 0.50

General Comments

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