Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_provenance.
- NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_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." NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_provenance.
- NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_assertion evidence source_evidence_literature NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_provenance.
- NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_assertion SIO_000772 21937582 NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_provenance.
- NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_assertion wasDerivedFrom befree-20140225 NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_provenance.
- NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_assertion wasGeneratedBy ECO_0000203 NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP487269.RAVC-26FS5xAK5tXTjz4yhxn4doJfAIB6BOduCkD1PUDs130_provenance.