INT180836

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Context Info
Confidence 0.15
First Reported 2005
Last Reported 2005
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.20
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.

pigmentation (NF1) signal transduction (NF1) nucleus (NF1)
intracellular (NF1) extracellular matrix organization (NF1) cytoplasm (NF1)
CTD (Homo sapiens)
NF1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Arthritis 1 27.36 Quite Low
Pain 4 11.00 Low Low
Osteoarthritis 3 5.00 Very Low Very Low Very Low
headache 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Cleidocranial Dysplasia 31 100.00 Very High Very High Very High
Watson Syndrome 30 100.00 Very High Very High Very High
Arthritis 1 27.36 Quite Low
Cognitive Disorder 3 12.84 Low Low
Pain 4 11.00 Low Low
Disease 12 5.00 Very Low Very Low Very Low
Pseudarthrosis 2 5.00 Very Low Very Low Very Low
Amputation 2 5.00 Very Low Very Low Very Low
Osteoarthritis 2 5.00 Very Low Very Low Very Low
Contracture 2 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
d) it includes many of the most important domains in the context of NF1-CTD;
CTD Binding (context) of NF1 associated with cleidocranial dysplasia and watson syndrome
1) Confidence 0.15 Published 2005 Journal Health Qual Life Outcomes Section Body Doc Link PMC548287 Disease Relevance 0.20 Pain Relevance 0

General Comments

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