Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_provenance.
- NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_assertion description "[Mutations in the KCNQ1, HERG, SCN5A, minK and MiRP1 genes cause long QT syndrome (LQTS), of which there are two forms: the Romano Ward syndrome and the Jervell and Lange-Nielsen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_provenance.
- NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_assertion evidence source_evidence_literature NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_provenance.
- NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_assertion SIO_000772 18752142 NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_provenance.
- NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_assertion wasDerivedFrom befree-20140225 NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_provenance.
- NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_assertion wasGeneratedBy ECO_0000203 NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP669509.RA0hjbP-5uhQ6Z519P3YBMbYL7Mog8YWD6CMT9FAdid7E130_provenance.