INT271962

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Context Info
Confidence 0.73
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.08
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.

transport (SLC7A6) plasma membrane (SLC7A6) protein complex assembly (SLC7A6)
transmembrane transport (SLC7A6) cellular amino acid metabolic process (SLC7A6)
SLC7A6 (Homo sapiens)
Pain Link Frequency Relevance Heat
cerebral cortex 1 5.00 Very Low Very Low Very Low
transdermal 1 5.00 Very Low Very Low Very Low
adenocard 1 5.00 Very Low Very Low Very Low
Angina 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Helminth Infection 1 76.68 Quite High
Tuberous Sclerosis 11 50.00 Quite Low
Sprains And Strains 3 33.76 Quite Low
Disease 21 5.00 Very Low Very Low Very Low
Cancer 20 5.00 Very Low Very Low Very Low
Angiomyolipoma 12 5.00 Very Low Very Low Very Low
Lymphangioleiomyomatosis 11 5.00 Very Low Very Low Very Low
Convulsion 9 5.00 Very Low Very Low Very Low
Hamartoma 8 5.00 Very Low Very Low Very Low
Anaplastic Astrocytoma 6 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Deletion of the TSC1 or TSC2 genes in this organism results in similar defects in the localization of amino acid permease, nutrient uptake and conjugation.
Localization (localization) of amino acid permease
1) Confidence 0.73 Published 2008 Journal Current Genomics Section Body Doc Link PMC2691673 Disease Relevance 0.08 Pain Relevance 0

General Comments

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