INT251522

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Context Info
Confidence 0.35
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 1
Disease Relevance 0.82
Pain Relevance 0.11

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

nucleus (MED13L)
Anatomy Link Frequency
thyroid 1
MED13L (Homo sapiens)
Pain Link Frequency Relevance Heat
antiepileptic Drug 2 99.04 Very High Very High Very High
palliative 5 58.40 Quite High
imagery 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Gestational Diabetes 2 95.56 Very High Very High Very High
Cv General 4 Under Development 6 91.32 High High
Cyanosis 8 86.12 High High
Ventricular Heart Septal Defects 13 85.72 High High
Congenital Anomalies 2 54.68 Quite High
Gynecomastia 3 53.16 Quite High
Cognitive Disorder 2 25.00 Low Low
Disease 7 5.00 Very Low Very Low Very Low
Cv General 2 Under Development 3 5.00 Very Low Very Low Very Low
Pathologic Constriction 3 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Mutations in growth differentiation factor-1 gene, the thyroid hormone receptor-associated protein-2 gene and the gene encoding the cryptic protein have been shown implicated in discordant VA connections, but they explain only a small minority of TGA cases.
Positive_regulation (Mutations) of thyroid hormone receptor-associated protein-2 gene in thyroid
1) Confidence 0.35 Published 2008 Journal Orphanet J Rare Dis Section Abstract Doc Link PMC2577629 Disease Relevance 0.82 Pain Relevance 0.11

General Comments

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