Matches in Nanopublications for { ?s ?p "[Defects in the newly reported gene NPHS1 in chromosome 19 cause the massive proteinuria of Finnish type congenital nephrotic syndrome (CNF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_assertion description "[Defects in the newly reported gene NPHS1 in chromosome 19 cause the massive proteinuria of Finnish type congenital nephrotic syndrome (CNF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance.