Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_provenance.
- NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_assertion description "[The frequency of the HLA-DRB1*07 allele was higher in the CSS patients than in controls (27.1% versus 13.3%; chi(2) = 12.64, P = 0.0003, corrected P [P(corr)] = 0.0042, odds ratio [OR] 2.42, 95% confidence interval [95% CI] 1.47-3.99).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_provenance.
- NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_assertion evidence source_evidence_literature NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_provenance.
- NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_assertion SIO_000772 17763415 NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_provenance.
- NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_assertion wasDerivedFrom befree-20150227 NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_provenance.
- NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_assertion wasGeneratedBy ECO_0000203 NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP454682.RA3_yNFMtV3lZQrCfY9jnJYFm33yx6UYNjqm4C8DiYXMg130_provenance.