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- NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_assertion type Assertion NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_head.
- NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_assertion wasGeneratedBy ECO_0000203 NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_provenance.
- NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_assertion wasDerivedFrom befree-20140225 NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_provenance.
- NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_assertion SIO_000772 12163457 NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_provenance.
- NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_assertion evidence source_evidence_literature NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_provenance.
- NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_assertion description "[Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273217.RAFsGuVpAvram6UT9B_cVdirQlOG0OHknUk5pzXdvIdJ4130_provenance.