INT131130

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Context Info
Confidence 0.01
First Reported 2005
Last Reported 2005
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 1
Disease Relevance 1.00
Pain Relevance 0.08

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

structural molecule activity (Krt16) plasma membrane (PKD1) nucleus (PKD1)
cilium (PKD1) cytoplasm (PKD1)
PKD1 (Homo sapiens)
Krt16 (Mus musculus)
Pain Link Frequency Relevance Heat
Pain 2 79.36 Quite High
Disease Link Frequency Relevance Heat
Pachyonychia Congenita 10 100.00 Very High Very High Very High
Skin Appendage Disease 1 69.44 Quite High
Oral Leukoplakia 1 67.76 Quite High
Darier's Disease 1 65.60 Quite High
Cyst 3 60.48 Quite High
Hoarseness 1 59.44 Quite High
Tooth Loss 1 52.48 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Pathogenic mutations in keratins K6a or K16 are associated with the PC-1 phenotype whereas K6b and K17 mutations are associated with the PC-2 phenotype.
PC-1 Binding (associated) of K16 associated with pachyonychia congenita
1) Confidence 0.01 Published 2005 Journal J. Investig. Dermatol. Symp. Proc. Section Abstract Doc Link 16250204 Disease Relevance 1.00 Pain Relevance 0.08

General Comments

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