Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_assertion> ?p ?o ?g. }
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- NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_assertion type Assertion NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_head.
- NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_assertion description "[Hereditary deficiency of C1 esterase inhibitor (C1 INH) responsible for hereditary angioedema (HAE) is the most common hereditary complement deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_provenance.
- NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_assertion evidence source_evidence_literature NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_provenance.
- NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_assertion SIO_000772 2736814 NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_provenance.
- NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_assertion wasDerivedFrom befree-2016 NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_provenance.
- NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_assertion wasGeneratedBy ECO_0000203 NP1296422.RAc9DltOWWH25sLs0OnKD9O0haYlnLFLD1fgNfeVEJGbs130_provenance.