Matches in Nanopublications for { ?s ?p "[Mutations in the ACTN4 gene cause focal segmental glomerulosclerosis (FSGS), which shows autosomal dominant inheritance (Online Mendelian Inheritance in Man No.603278, FSGS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_assertion description "[Mutations in the ACTN4 gene cause focal segmental glomerulosclerosis (FSGS), which shows autosomal dominant inheritance (Online Mendelian Inheritance in Man No.603278, FSGS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_provenance.