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Context Info
Confidence 0.27
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.37
Pain Relevance 0.08

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

cell differentiation (MYT1) nucleus (MYT1) DNA binding (MYT1)
MYT1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Neuronal excitability 1 79.92 Quite High
Central nervous system 1 79.12 Quite High
Pain 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Convulsion 16 82.24 Quite High
Epilepsy 6 76.04 Quite High
Anxiety Disorder 2 72.92 Quite High
Targeted Disruption 1 71.76 Quite High
Frontal Lobe Epilepsy 1 49.28 Quite Low
Benign Neonatal Epilepsy 1 46.80 Quite Low
Neurological Disease 1 38.96 Quite Low
Cognitive Disorder 3 36.16 Quite Low
Partial Seizures 2 34.16 Quite Low
Fever 2 25.64 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The smallest 20q13.33 microdeletion, report by Kroepfl and colleagues [8], is a subtelomere microdeletion encompassing only two genes, myelin transcription factor 1 (MYTI) and protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2 (PCMTD2) (Figure 1).
Transcription (transcription) of MYTI
1) Confidence 0.27 Published 2010 Journal PLoS ONE Section Body Doc Link PMC2929201 Disease Relevance 0.37 Pain Relevance 0.08

General Comments

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