Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_provenance.
- NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_assertion description "[Variants in SCN5A and KCNH2, disease genes for long QT and Brugada syndromes, were assessed for potential pathogenicity by 3 laboratories with ion channel expertise and by comparison with the ClinVar database.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_provenance.
- NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_assertion evidence source_evidence_literature NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_provenance.
- NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_assertion SIO_000772 26746457 NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_provenance.
- NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_assertion wasDerivedFrom befree-2016 NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_provenance.
- NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_assertion wasGeneratedBy ECO_0000203 NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_provenance.