Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_assertion> ?p ?o ?g. }
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- NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_assertion type Assertion NP1295904.RAvqvoxPJOCn0ai1B6pmWgJpXDY21XR4e_jjH3wIXY5zA130_head.
- 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.