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- NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_assertion type Assertion NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_head.
- NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_assertion wasGeneratedBy ECO_0000203 NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_provenance.
- NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_assertion wasDerivedFrom befree-20140225 NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_provenance.
- NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_assertion SIO_000772 10688323 NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_provenance.
- NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_assertion evidence source_evidence_literature NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_provenance.
- NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_provenance.