Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_assertion> ?p ?o ?g. }
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- NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_assertion type Assertion NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_head.
- 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.
- NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_assertion evidence source_evidence_literature NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_provenance.
- NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_assertion SIO_000772 7742232 NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_provenance.
- NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_assertion wasDerivedFrom befree-20150227 NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_provenance.
- NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_assertion wasGeneratedBy ECO_0000203 NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_provenance.