Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682452.RAu3ebn1YJWxzxDAHDeMicZgmHLYiJn_R27-ysePEVXFU130_provenance.
- 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.