Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_provenance.
- NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_assertion description "[We then genotyped 37 SNPs in or near PTPN22 in 475 patients with RA and 475 individually matched controls (sample set 1) and selected a subset of markers for replication in an additional 661 patients with RA and 1,322 individually matched controls (sample set 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_provenance.
- NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_assertion evidence source_evidence_literature NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_provenance.
- NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_assertion SIO_000772 16175503 NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_provenance.
- NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_assertion wasDerivedFrom befree-2016 NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_provenance.
- NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_assertion wasGeneratedBy ECO_0000203 NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_provenance.
- befree-2016 importedOn "2016-02-19" NP514458.RA3iW7H_W5zUo8P5s5sus6rPgUTD9R3r5puw3wqCPPWOc130_provenance.