Matches in Nanopublications for { ?s ?p "[Andersen syndrome (AS) is a rare genetic disease caused by mutations of the potassium channel Kir2.1 (KCNJ2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP211945.RAITsGlYACod6_RSlgyCTKIa7LXHjLVtf8-ffo71JyT78130_assertion description "[Andersen syndrome (AS) is a rare genetic disease caused by mutations of the potassium channel Kir2.1 (KCNJ2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211945.RAITsGlYACod6_RSlgyCTKIa7LXHjLVtf8-ffo71JyT78130_provenance.
- assertion description "[Andersen syndrome (AS) is a rare genetic disease caused by mutations of the potassium channel Kir2.1 (KCNJ2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Andersen syndrome (AS) is a rare genetic disease caused by mutations of the potassium channel Kir2.1 (KCNJ2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.