Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_provenance.
- NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_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." NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_provenance.
- NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_assertion evidence source_evidence_literature NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_provenance.
- NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_assertion SIO_000772 15466643 NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_provenance.
- NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_assertion wasDerivedFrom befree-20140225 NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_provenance.
- NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_assertion wasGeneratedBy ECO_0000203 NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP865217.RA8DvZDXrbnthptU6s1F4T0c8WnIxwtLstCEGDKd_o5t8130_provenance.