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- source_evidence_literature type ECO_0000212 NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_provenance.
- befree-2016 importedOn "2016-02-19" NP431396.RAvIT9tbvzhWeKuuEkbu-FT4tbUQo3ihHahTMJ2D0Ao4I130_provenance.
- 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.