Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_assertion> ?p ?o ?g. }
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- NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_assertion type Assertion NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_head.
- NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_assertion description "[We studied a large Swiss family with dominantly inherited hereditary spherocytosis and band 3 (anion exchanger 1, AE1) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_provenance.
- NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_assertion evidence source_evidence_literature NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_provenance.
- NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_assertion SIO_000772 8547122 NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_provenance.
- NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_assertion wasDerivedFrom befree-2016 NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_provenance.
- NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_assertion wasGeneratedBy ECO_0000203 NP1344974.RACyxl0mwMnl1EtW5UElQhjjhgLakt7m7xBwOaIE7KQyY130_provenance.