Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_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.
- 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.
- befree-20150227 importedOn "2015-02-27" NP233673.RAz-bL73EQcB9vlwjyR2DavnAMoXJoJ6xTvfRk5LXPIWM130_provenance.