Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_provenance.
- NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_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." NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_provenance.
- NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_assertion evidence source_evidence_literature NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_provenance.
- NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_assertion SIO_000772 17200162 NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_provenance.
- NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_assertion wasDerivedFrom befree-20140225 NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_provenance.
- NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_assertion wasGeneratedBy ECO_0000203 NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP250627.RAgPAJoj4BvL_-VwxFWliSePMf0fNTme18Y8if3r-0EFI130_provenance.