Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_assertion> ?p ?o ?g. }
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- NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_assertion type Assertion NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_head.
- NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_assertion wasGeneratedBy ECO_0000203 NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_provenance.
- NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_assertion wasDerivedFrom befree-2016 NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_provenance.
- NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_assertion SIO_000772 14872505 NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_provenance.
- NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_assertion evidence source_evidence_literature NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_provenance.
- NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_assertion description "[Mutations in the NALP3/CIAS1/PYPAF1 gene are associated with the autoinflammatory diseases Muckle-Wells syndrome (MWS), familial cold autoinflammatory syndrome (FCAS), and neonatal-onset multisystem inflammatory disease (NOMID), which is also known as chronic infantile neurologic, cutaneous, articular (CINCA) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_provenance.