Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_assertion> ?p ?o ?g. }
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- NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_assertion type Assertion NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_head.
- NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_assertion wasGeneratedBy ECO_0000203 NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_provenance.
- NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_assertion wasDerivedFrom lhgdn-20090331 NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_provenance.
- NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_assertion SIO_000772 12163457 NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_provenance.
- NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_assertion evidence source_evidence_literature NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_provenance.
- NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_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." NP153614.RAaK9SR_SEEY6etTEsKTKM4aJfg59c900iGOEi2KeGnQM130_provenance.