INT135056

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Context Info
Confidence 0.21
First Reported 2006
Last Reported 2006
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 1
Disease Relevance 0.69
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.

signal transduction (MTSS1) cell adhesion (MTSS1) cytoplasm (MTSS1)
MTSS1 (Homo sapiens)
Pain Link Frequency Relevance Heat
anesthesia 1 25.00 Low Low
Disease Link Frequency Relevance Heat
Primary Hyperoxaluria 1 100.00 Very High Very High Very High
Hyperoxaluria 7 97.28 Very High Very High Very High
Nephrocalcinosis 3 96.68 Very High Very High Very High
Renal Insufficiency 2 95.80 Very High Very High Very High
Peroxisomal Disorder 1 75.00 Quite High
Urolithiasis 1 30.40 Quite Low
Renal Disease 1 25.00 Low Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Its deficiency causes primary hyperoxaluria type 1 (PH1, MIM 259900), an inborn error of glyoxylate metabolism characterized by hyperoxaluria, nephrocalcinosis, and renal insufficiency.
Positive_regulation (causes) of MIM associated with renal insufficiency, nephrocalcinosis, hyperoxaluria and primary hyperoxaluria
1) Confidence 0.21 Published 2006 Journal Mol. Genet. Metab. Section Abstract Doc Link 16621644 Disease Relevance 0.69 Pain Relevance 0

General Comments

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