INT131674

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Context Info
Confidence 0.10
First Reported 2005
Last Reported 2010
Negated 0
Speculated 0
Reported most in Abstract
Documents 3
Total Number 3
Disease Relevance 3.78
Pain Relevance 0.32

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

small molecule metabolic process (HEXB) cell death (HEXB) carbohydrate metabolic process (HEXB)
lysosome (HEXB)
HEXB (Homo sapiens)
Pain Link Frequency Relevance Heat
methotrexate 5 97.60 Very High Very High Very High
Bile 1 78.64 Quite High
peripheral neuropathy 3 64.32 Quite High
abdominal pain 2 59.40 Quite High
depression 6 57.12 Quite High
Peripheral nervous system 1 7.48 Low Low
gABA 18 5.00 Very Low Very Low Very Low
Dopamine 14 5.00 Very Low Very Low Very Low
Glutamate 8 5.00 Very Low Very Low Very Low
agonist 5 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Disease 22 99.38 Very High Very High Very High
Ataxia 73 94.96 High High
Reprotox - General 2 14 94.76 High High
Van Bogaert's Disease 5 93.28 High High
Hypoalbuminemia 1 91.80 High High
Telangiectasia 2 79.80 Quite High
Disorder Of Lipid Metabolism 1 77.28 Quite High
Hypolipidemia 4 74.68 Quite High
Dementia 1 74.32 Quite High
Syndrome 9 71.40 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Expectant management is appropriate only when beta subunit of human chorionic gonadotropin levels are low and declining.
Negative_regulation (low) of beta subunit
1) Confidence 0.10 Published 2005 Journal Am Fam Physician Section Abstract Doc Link 16300032 Disease Relevance 0.83 Pain Relevance 0.11
Expectant management is appropriate only when beta subunit of human chorionic gonadotropin levels are low and declining.
Negative_regulation (declining) of beta subunit
2) Confidence 0.10 Published 2005 Journal Am Fam Physician Section Abstract Doc Link 16300032 Disease Relevance 0.83 Pain Relevance 0.11
Late-onset Tay-Sachs disease (LOTSD) is characterized by a deficiency in beta-hexosaminidase due to a mutation in the HEXA gene [149].
Negative_regulation (deficiency) of beta-hexosaminidase associated with disease
3) Confidence 0.01 Published 2010 Journal Current Neuropharmacology Section Body Doc Link PMC2866461 Disease Relevance 2.11 Pain Relevance 0.10

General Comments

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