INT95757

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Context Info
Confidence 0.41
First Reported 2001
Last Reported 2001
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 2
Disease Relevance 1.05
Pain Relevance 0.21

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

cytoskeleton (UBXN11) cytoplasm (UBXN11)
UBXN11 (Homo sapiens)
Pain Link Frequency Relevance Heat
anesthesia 2 70.16 Quite High
imagery 2 66.32 Quite High
Disease Link Frequency Relevance Heat
Adrenoleukodystrophy 6 95.96 Very High Very High Very High
Muscle Hypotonia 2 76.16 Quite High
Convulsion 2 74.56 Quite High
Ocular Toxicity (including Many Sub-types) 4 72.40 Quite High
Disease 2 60.08 Quite High
Neurological Disease 2 51.68 Quite High
Cognitive Disorder 2 49.20 Quite Low
Neuropathic Pain 2 42.40 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The disorders of peroxisomal beta-oxidation, which have been well characterised at the molecular level, include defects of acyl-CoA oxidase, defects of the D-bifunctional protein (D-BP) (including specific defects of its enoyl-CoA hydratase and D-3-hydroxyacyl-CoA dehydrogenase components), defects of the very-long-chain fatty acid (VLCFA)-CoA importer [X-linked adrenoleukodystrophy (ALD)] and alpha-methylacyl-CoA racemase deficiency.
Negative_regulation (defects) of Gene_expression (defects) of CoA associated with adrenoleukodystrophy
1) Confidence 0.41 Published 2001 Journal Biochem. Soc. Trans. Section Abstract Doc Link 11356171 Disease Relevance 0.53 Pain Relevance 0.10
The disorders of peroxisomal beta-oxidation, which have been well characterised at the molecular level, include defects of acyl-CoA oxidase, defects of the D-bifunctional protein (D-BP) (including specific defects of its enoyl-CoA hydratase and D-3-hydroxyacyl-CoA dehydrogenase components), defects of the very-long-chain fatty acid (VLCFA)-CoA importer [X-linked adrenoleukodystrophy (ALD)] and alpha-methylacyl-CoA racemase deficiency.
Negative_regulation (defects) of Gene_expression (defects) of CoA associated with adrenoleukodystrophy
2) Confidence 0.41 Published 2001 Journal Biochem. Soc. Trans. Section Abstract Doc Link 11356171 Disease Relevance 0.53 Pain Relevance 0.10

General Comments

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