Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_assertion> ?p ?o ?g. }
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- NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_assertion type Assertion NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_head.
- NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_assertion wasGeneratedBy ECO_0000203 NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_provenance.
- NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_assertion wasDerivedFrom befree-20150227 NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_provenance.
- NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_assertion SIO_000772 21844054 NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_provenance.
- NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_assertion evidence source_evidence_literature NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_provenance.
- NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_assertion description "[It was reported recently that a proportion of patients previously diagnosed with alleged vaccine encephalopathy might possess SCN1A mutations and clinical histories that enabled a diagnosis of Dravet syndrome, but these results have not been replicated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_provenance.