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- source_evidence_literature type ECO_0000212 NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_provenance.
- NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_assertion wasGeneratedBy ECO_0000203 NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_provenance.
- NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_assertion wasDerivedFrom befree-20150227 NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_provenance.
- NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_assertion SIO_000772 14872505 NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_provenance.
- NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_assertion evidence source_evidence_literature NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_provenance.
- NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_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." NP964729.RAI6wojYDQW6OwUHdhl9gCsPHPtkRNcHov7Ywqbpfin_s130_provenance.