Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_provenance.
- NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_assertion description "[We demonstrate a significantly increased frequency of low IL-10 expressing -1082A/A alleles, the medium IL-10 expressing ACC haplotype (p=0.01), and an enrichment of the rare GTC haplotype (p<0.001) in patients with SoJIA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_provenance.
- NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_assertion evidence source_evidence_literature NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_provenance.
- NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_assertion SIO_000772 21205466 NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_provenance.
- NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_assertion wasDerivedFrom befree-20140225 NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_provenance.
- NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_assertion wasGeneratedBy ECO_0000203 NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP870519.RANNNY0K9Dvw6-OxQeY7jiUB5kn_ELflT2g18ZBq_oBRo130_provenance.