Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_provenance.
- NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_assertion description "[Analysis of the HLA typing results showed that the relative risk (RR) of 4.00 95% confidence interval (95% CI) 1.20-13.28, two-tailed P = 0.018 for allele HLA-DQB1*04 class II, detected in 33.3% of PR patients, was significant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_provenance.
- NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_assertion evidence source_evidence_literature NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_provenance.
- NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_assertion SIO_000772 16405603 NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_provenance.
- NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_assertion wasDerivedFrom gad-20150221 NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_provenance.
- NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_assertion wasGeneratedBy ECO_0000203 NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP84048.RAYLnlvO7Jm1NvNUVdulQQhG_Hi-rp9xgcd2ra1-wPJSA130_provenance.