Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_assertion> ?p ?o ?g. }
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- NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_assertion type Assertion NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_head.
- 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.
- NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_assertion evidence source_evidence_literature NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_provenance.
- NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_assertion SIO_000772 7742232 NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_provenance.
- NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_assertion wasDerivedFrom befree-20140225 NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_provenance.
- NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_assertion wasGeneratedBy ECO_0000203 NP886357.RAlwG3dgIRSp4CB56HRhFxh3bGa7rU0nJRrqm7rHqC4fI130_provenance.