Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_provenance.
- NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_assertion description "[Investigating all common variants in IL1A, IL1B, IL1RN,IL6 and IL10 genes revealed a statistically significant association (rs452204 p(empirical) = 0.02) with one IL1RN variant and ESRD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_provenance.
- NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_assertion evidence source_evidence_literature NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_provenance.
- NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_assertion SIO_000772 20551628 NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_provenance.
- NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_assertion wasDerivedFrom befree-20140225 NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_provenance.
- NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_assertion wasGeneratedBy ECO_0000203 NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP887718.RAcwtaRb9v7rr1b7B5R_l1l2gwaJ8vNJ6-ed0ZyUg2t-8130_provenance.