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- NP182514.RAJtkHB4pyyS-6k-GJzMXoWQpDwpURm8R0l6q--KM14Mw130_assertion type Assertion NP182514.RAJtkHB4pyyS-6k-GJzMXoWQpDwpURm8R0l6q--KM14Mw130_head.
- 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.
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- NP182514.RAJtkHB4pyyS-6k-GJzMXoWQpDwpURm8R0l6q--KM14Mw130_assertion wasDerivedFrom befree-20140225 NP182514.RAJtkHB4pyyS-6k-GJzMXoWQpDwpURm8R0l6q--KM14Mw130_provenance.
- NP182514.RAJtkHB4pyyS-6k-GJzMXoWQpDwpURm8R0l6q--KM14Mw130_assertion wasGeneratedBy ECO_0000203 NP182514.RAJtkHB4pyyS-6k-GJzMXoWQpDwpURm8R0l6q--KM14Mw130_provenance.