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- NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_assertion type Assertion NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_head.
- NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_assertion wasGeneratedBy ECO_0000203 NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_provenance.
- NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_assertion wasDerivedFrom befree-2016 NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_provenance.
- NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_assertion SIO_000772 22401837 NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_provenance.
- NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_assertion evidence source_evidence_literature NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_provenance.
- NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_assertion description "[Medical conditions associated with catatonia included auto-immune encephalitis (systemic lupus erythematosus [N=3] and anti-NMDA-receptor encephalitis [N=1]), seizures (N=1), ciclosporin encephalitis (N=1), post hypoglycaemic coma encephalitis (N=1), and genetic or metabolic conditions (chorea [N=2], 5HT cerebrospinal fluid deficit [N=1], storage disease [N=1], fatal familial insomnia [FFI; N=1], and PRODH mutations [N=1]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966322.RAPFcckkipbAgPyw_MMM1jyjkCCvCvH1m-UbemcRobK44130_provenance.