Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_provenance.
- NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_assertion description "[This region also contains a locus for right ventricular cardiomyopathy (ARVD5) and the cardiac sodium channel gene (SCN5A), mutations that cause isolated progressive cardiac conduction defect (Lenegre syndrome), long-QT syndrome (LQT3), and Brugada syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_provenance.
- NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_assertion evidence source_evidence_literature NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_provenance.
- NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_assertion SIO_000772 15466643 NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_provenance.
- NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_assertion wasDerivedFrom befree-20140225 NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_provenance.
- NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_assertion wasGeneratedBy ECO_0000203 NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP786255.RAKp20SH6-_MKtxHtlizhaw6NSGHu1SUbZvVJ2khEHICA130_provenance.