Matches in Nanopublications for { ?s ?p "[Congenital nephrotic syndrome of the Finnish type (NPHS1, CNF) is an autosomal recessively inherited disease occurring due to mutations in the nephrin gene (NPHS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_assertion description "[Congenital nephrotic syndrome of the Finnish type (NPHS1, CNF) is an autosomal recessively inherited disease occurring due to mutations in the nephrin gene (NPHS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_provenance.
- NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_assertion description "[Congenital nephrotic syndrome of the Finnish type (NPHS1, CNF) is an autosomal recessively inherited disease occurring due to mutations in the nephrin gene (NPHS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_provenance.