Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_provenance.
- NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_assertion wasGeneratedBy ECO_0000203 NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_provenance.
- NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_assertion wasDerivedFrom befree-20140225 NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_provenance.
- NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_assertion SIO_000772 21844054 NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_provenance.
- NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_assertion evidence source_evidence_literature NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_provenance.
- NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_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." NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP610923.RAqFVJQ3wl_V4Xn-osTXdNgN2GmwEEFrWmm-CQ9AJ0VJQ130_provenance.