Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_provenance.
- NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_assertion description "[Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_provenance.
- NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_assertion evidence source_evidence_literature NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_provenance.
- NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_assertion SIO_000772 23872634 NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_provenance.
- NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_assertion wasDerivedFrom befree-20150227 NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_provenance.
- NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_assertion wasGeneratedBy ECO_0000203 NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683559.RA5EzuUXOc9Stv_tr70Z221XGWlHHtKI7JEpegTjntjW4130_provenance.