Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_provenance.
- NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_assertion description "[This study confirms that ARX is involved in the pathogenesis of cryptogenic early onset epileptic encephalopathy, such as OS, and suggests that the severity of the electroclinical picture is likely to not exclusively correlate with the extent of expansions of the polyalanine tracts, but rather with the functional effect of different pathogenetic mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_provenance.
- NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_assertion evidence source_evidence_literature NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_provenance.
- NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_assertion SIO_000772 21108397 NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_provenance.
- NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_assertion wasDerivedFrom befree-20140225 NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_provenance.
- NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_assertion wasGeneratedBy ECO_0000203 NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP218891.RAdSnOPVpTb_atH8X4J0VvAlijH8lPlq4Og4SvuR5KkTA130_provenance.