Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion type Assertion NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_head.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_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." NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion evidence source_evidence_literature NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion SIO_000772 10688323 NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion wasDerivedFrom befree-20140225 NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion wasGeneratedBy ECO_0000203 NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.