INT213615

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Context Info
Confidence 0.73
First Reported 2007
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 2
Total Number 2
Disease Relevance 0.61
Pain Relevance 0.17

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

plasma membrane (NPSR1) cytoplasm (NPSR1) signal transducer activity (NPSR1)
NPSR1 (Homo sapiens)
Pain Link Frequency Relevance Heat
rheumatoid arthritis 42 98.04 Very High Very High Very High
Neuropeptide 12 84.00 Quite High
cytokine 2 77.36 Quite High
Arthritis 12 34.92 Quite Low
Opioid 1 18.64 Low Low
Inflammation 14 5.00 Very Low Very Low Very Low
adenocard 2 5.00 Very Low Very Low Very Low
dopamine receptor 1 5.00 Very Low Very Low Very Low
Locus ceruleus 1 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Rheumatoid Arthritis 53 98.04 Very High Very High Very High
Sleep Disorders 55 86.04 High High
Disease 20 74.00 Quite High
Apnoea 3 44.48 Quite Low
Snoring 3 43.68 Quite Low
Inflammatory Bowel Disease 7 28.28 Quite Low
Asthma 7 27.96 Quite Low
Adhesions 1 16.40 Low Low
INFLAMMATION 12 5.00 Very Low Very Low Very Low
Chronobiology Disorders 2 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
No other associations were detected either with single markers or when NPSR1 haplotypes were inferred from individual SNP genotypes, in RA as a whole or when patients were subdivided into phenotypic groups as described above (not shown).
Localization (haplotypes) of NPSR1 associated with rheumatoid arthritis
1) Confidence 0.73 Published 2010 Journal PLoS ONE Section Body Doc Link PMC2825264 Disease Relevance 0.39 Pain Relevance 0.09
Only one of these is located in a coding region: rs324981 in NPSR1, associated with usual bedtime, whose minor allele (frequency 0.44) is a non-synonymous mutation encoding an Asn107?
Localization (located) of NPSR1
2) Confidence 0.69 Published 2007 Journal BMC Med Genet Section Body Doc Link PMC1995620 Disease Relevance 0.22 Pain Relevance 0.08

General Comments

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