Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP713639.RApXdLG4KIw8h0ydT3x85UuyylMLuukxGYbDMHZDcYuBI130_provenance.