Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_provenance.
- NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_assertion description "[Mutations in the gene-encoding Na(v)1.5, SCN5A, have been associated with a variety of arrhythmic disorders, including long QT, Brugada, and sick sinus syndromes as well as progressive cardiac conduction defect and atrial standstill.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_provenance.
- NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_assertion evidence source_evidence_literature NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_provenance.
- NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_assertion SIO_000772 21937582 NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_provenance.
- NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_assertion wasDerivedFrom befree-2016 NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_provenance.
- NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_assertion wasGeneratedBy ECO_0000203 NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_provenance.
- befree-2016 importedOn "2016-02-19" NP925496.RARq_TKDE-KYnNsSqPs0GAtM31DT68SXxYuEUEFXMlsh0130_provenance.