INT111345

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Context Info
Confidence 0.30
First Reported 2003
Last Reported 2003
Negated 0
Speculated 0
Reported most in Abstract
Documents 2
Total Number 3
Disease Relevance 2.82
Pain Relevance 0.36

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

cytosol (Cbs) lyase activity (Cbs) nucleolus (Cbs)
nucleus (Cbs) enzyme binding (Cbs) cytoplasm (Cbs)
Anatomy Link Frequency
blood 1
brain 1
Cbs (Rattus norvegicus)
Pain Link Frequency Relevance Heat
anesthesia 5 86.80 High High
Hippocampus 6 75.00 Quite High
Disease Link Frequency Relevance Heat
Inborn Error Of Metabolism 1 99.64 Very High Very High Very High
Homocystinuria 11 98.98 Very High Very High Very High
Metabolic Disorder 2 98.04 Very High Very High Very High
Intellectual Impairment 2 97.04 Very High Very High Very High
Convulsion 2 95.44 Very High Very High Very High
Increased Venous Pressure Under Development 6 94.32 High High
Stress 8 92.16 High High
Neurodegenerative Disease 2 87.44 High High
Disease 2 82.80 Quite High
Stroke 2 82.08 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Homocystinuria is an inborn error of metabolism caused by severe deficiency of cystathionine beta-synthase activity.
Negative_regulation (deficiency) of cystathionine beta-synthase associated with inborn error of metabolism and homocystinuria
1) Confidence 0.30 Published 2003 Journal Neurochem. Int. Section Abstract Doc Link 12820989 Disease Relevance 0.27 Pain Relevance 0.15
Homocystinuria is an inherited metabolic disease characterized biochemically by increased blood and brain levels of homocysteine caused by severe deficiency of cystathionine beta-synthase activity.
Negative_regulation (deficiency) of cystathionine beta-synthase in brain associated with metabolic disorder and homocystinuria
2) Confidence 0.24 Published 2003 Journal Metab Brain Dis Section Abstract Doc Link 12822833 Disease Relevance 1.27 Pain Relevance 0.10
Homocystinuria is an inherited metabolic disease characterized biochemically by increased blood and brain levels of homocysteine caused by severe deficiency of cystathionine beta-synthase activity.
Negative_regulation (deficiency) of cystathionine beta-synthase in blood associated with metabolic disorder and homocystinuria
3) Confidence 0.08 Published 2003 Journal Metab Brain Dis Section Abstract Doc Link 12822833 Disease Relevance 1.27 Pain Relevance 0.10

General Comments

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