Matches in Nanopublications for { ?s ?p "[Type 2 congenital long-QT syndrome (LQT2) results from KCNH2 mutations that cause loss of Kv11.1 channel function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 3 of
3
with 100 items per page.
- NP182514.RAJtkHB4pyyS-6k-GJzMXoWQpDwpURm8R0l6q--KM14Mw130_assertion description "[Type 2 congenital long-QT syndrome (LQT2) results from KCNH2 mutations that cause loss of Kv11.1 channel function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182514.RAJtkHB4pyyS-6k-GJzMXoWQpDwpURm8R0l6q--KM14Mw130_provenance.
- assertion description "[Type 2 congenital long-QT syndrome (LQT2) results from KCNH2 mutations that cause loss of Kv11.1 channel function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Type 2 congenital long-QT syndrome (LQT2) results from KCNH2 mutations that cause loss of Kv11.1 channel function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.