Matches in Nanopublications for { ?s ?p "[Congenital nephrotic syndrome of the Finnish type (CNF) is a rare autosomal recessively inherited disease characterised by intrauterine onset of massive urinary loss of proteins, 90% of which is albumin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_assertion description "[Congenital nephrotic syndrome of the Finnish type (CNF) is a rare autosomal recessively inherited disease characterised by intrauterine onset of massive urinary loss of proteins, 90% of which is albumin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_provenance.
- NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_assertion description "[Congenital nephrotic syndrome of the Finnish type (CNF) is a rare autosomal recessively inherited disease characterised by intrauterine onset of massive urinary loss of proteins, 90% of which is albumin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance.
- NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_assertion description "[Congenital nephrotic syndrome of the Finnish type (CNF) is a rare autosomal recessively inherited disease characterised by intrauterine onset of massive urinary loss of proteins, 90% of which is albumin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_provenance.