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- Q1771331 subject Q6853484.
- Q1771331 subject Q8279947.
- Q1771331 abstract "Cryopyrin-associated periodic syndrome (CAPS) is a spectrum of autoinflammatory syndromes including familial cold autoinflammatory syndrome (FCAS, formerly termed familial cold-induced urticaria), the Muckle-Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disease (NOMID, also called chronic infantile neurologic cutaneous and articular syndrome or CINCA). They share many clinical features.These syndromes are associated with mutations in NLRP3, the gene encoding cryopyrin. This is a component of the interleukin 1 inflammasome, and mutations lead to unregulated production of interleukin 1β. Monoclonal antibodies against interleukin 1β (such as canakinumab), other interleukin 1 binding proteins (such as rilonacept), or interleukin 1 receptor antagonist (for example anakinra) can be used to treat these disorders.".
- Q1771331 meshId "D056587".
- Q1771331 wikiPageExternalLink capsguide.php.
- Q1771331 wikiPageExternalLink 20140476.
- Q1771331 wikiPageWikiLink Q14905618.
- Q1771331 wikiPageWikiLink Q1538218.
- Q1771331 wikiPageWikiLink Q1706141.
- Q1771331 wikiPageWikiLink Q3278145.
- Q1771331 wikiPageWikiLink Q3552503.
- Q1771331 wikiPageWikiLink Q3655009.
- Q1771331 wikiPageWikiLink Q412405.
- Q1771331 wikiPageWikiLink Q415411.
- Q1771331 wikiPageWikiLink Q6853484.
- Q1771331 wikiPageWikiLink Q7334300.
- Q1771331 wikiPageWikiLink Q779203.
- Q1771331 wikiPageWikiLink Q8279947.
- Q1771331 meshid "D056587".
- Q1771331 name "Cryopyrin-associated periodic syndrome".
- Q1771331 type Disease.
- Q1771331 type Thing.
- Q1771331 type Q12136.
- Q1771331 comment "Cryopyrin-associated periodic syndrome (CAPS) is a spectrum of autoinflammatory syndromes including familial cold autoinflammatory syndrome (FCAS, formerly termed familial cold-induced urticaria), the Muckle-Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disease (NOMID, also called chronic infantile neurologic cutaneous and articular syndrome or CINCA). They share many clinical features.These syndromes are associated with mutations in NLRP3, the gene encoding cryopyrin.".
- Q1771331 label "Cryopyrin-associated periodic syndrome".
- Q1771331 name "Cryopyrin-associated periodic syndrome".