Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_provenance.
- NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_assertion description "[There was nominal evidence for allelic association at the marker FCRL3_8 in Graves' disease (OR, 1.50; 5-95% CIs, 1.06-2.13) and at FCRL3_9 with RA (OR, 1.25; 5-95% CIs, 1.01-1.54).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_provenance.
- NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_assertion evidence source_evidence_literature NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_provenance.
- NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_assertion SIO_000772 17200162 NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_provenance.
- NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_assertion wasDerivedFrom befree-20150227 NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_provenance.
- NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_assertion wasGeneratedBy ECO_0000203 NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP965533.RA6wqIBWbToQofgp3bPFZDX9jOqcXGJQvL4nUjyW-YMlQ130_provenance.