Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_assertion> ?p ?o ?g. }
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- NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_assertion type Assertion NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_head.
- NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_assertion description "[Compared with healthy control subjects, the heterozygous FCGR2A(c.742+871A>G) mutation was more frequent in patients with CVID (n = 53, P < .013).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_provenance.
- NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_assertion evidence source_evidence_literature NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_provenance.
- NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_assertion SIO_000772 23545275 NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_provenance.
- NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_assertion wasDerivedFrom befree-20140225 NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_provenance.
- NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_assertion wasGeneratedBy ECO_0000203 NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_provenance.