Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_provenance.
- NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_assertion description "[Most patients with PCDH19 mutations exhibit a distinctive electroclinical pattern of focal seizures with affective symptoms, suggesting an epileptogenic dysfunction involving the frontotemporal limbic system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_provenance.
- NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_assertion evidence source_evidence_literature NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_provenance.
- NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_assertion SIO_000772 22946748 NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_provenance.
- NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_assertion wasDerivedFrom befree-20140225 NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_provenance.
- NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_assertion wasGeneratedBy ECO_0000203 NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_provenance.
- befree-20140225 importedOn "2014-02-25" NP245962.RAAQgbiFyEYZ_qs5Y1VQXPoLytUym8qndOBlsVxX1-SME130_provenance.