Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_provenance.
- NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_assertion description "[Andersen-Tawil syndrome, a skeletal muscle syndrome associated with periodic paralysis and long QT intervals on the ECG, has been linked to defects in KCNJ2, the gene encoding for the inward rectifier potassium channel (I(K1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_provenance.
- NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_assertion evidence source_evidence_literature NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_provenance.
- NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_assertion SIO_000772 16500306 NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_provenance.
- NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_assertion wasDerivedFrom befree-20140225 NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_provenance.
- NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_assertion wasGeneratedBy ECO_0000203 NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP926558.RAKi21mMdb_3uEVn-LqU9OP9i7IpiykdUyEfbhcgYzjQM130_provenance.