INT268374

From wiki-pain
Jump to: navigation, search
Context Info
Confidence 0.37
First Reported 2005
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 2
Total Number 3
Disease Relevance 6.60
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.

peptidase activity (FAP) extracellular space (FAP) plasma membrane (FAP)
Anatomy Link Frequency
Juvenile 1
germline 1
FAP (Homo sapiens)
Pain Link Frequency Relevance Heat
abdominal pain 7 23.20 Low Low
COX2 7 5.00 Very Low Very Low Very Low
cINOD 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Colorectal Cancer 152 100.00 Very High Very High Very High
Familial Adenomatous Polyposis 142 100.00 Very High Very High Very High
Hereditary Nonpolyposis Colorectal Neoplasms 25 100.00 Very High Very High Very High
Syndrome 72 99.40 Very High Very High Very High
Hamartoma 3 98.80 Very High Very High Very High
Stomach Cancer 18 97.08 Very High Very High Very High
Hyperplasia 15 96.72 Very High Very High Very High
Disease 2 96.56 Very High Very High Very High
Endometriosis (extended) 12 95.52 Very High Very High Very High
Adenoma 37 89.08 High High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Familial adenomatous polyposis (FAP)
Gene_expression (polyposis) of FAP associated with familial adenomatous polyposis
1) Confidence 0.37 Published 2005 Journal Hered Cancer Clin Pract Section Body Doc Link PMC2837058 Disease Relevance 1.87 Pain Relevance 0
Gan Yuebo et al. [59] first reported an APC germline mutation in Chinese FAP patients in 1994.
Gene_expression (mutation) of FAP in germline associated with familial adenomatous polyposis
2) Confidence 0.32 Published 2005 Journal Hered Cancer Clin Pract Section Body Doc Link PMC2837058 Disease Relevance 2.03 Pain Relevance 0
Initial studies have concentrated on the molecular and genomic changes in easily characterisable inherited colorectal cancer syndromes such as Familial Adenomatous Polyposis (FAP), Lynch Syndrome (also known as Hereditary Non-Polyposis Colorectal Cancer, HNPCC), the more recently characterised MYH polyposis, Peutz-Jegher Syndrome, PTEN Hamartoma Syndrome, Juvenile Polyposis Syndrome and Hyperplastic Polyposis Syndrome.
Gene_expression (polyposis) of FAP in Juvenile associated with colorectal cancer, hamartoma, syndrome, familial adenomatous polyposis, hyperplasia and hereditary nonpolyposis colorectal neoplasms
3) Confidence 0.19 Published 2008 Journal Current Genomics Section Body Doc Link PMC2674304 Disease Relevance 2.71 Pain Relevance 0

General Comments

This test has worked.

Personal tools
Namespaces

Variants
Actions
Navigation
Toolbox