Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_provenance.
- NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_assertion description "[The relative risk of acute GVHD associated with a single locus HLA-DQB1 mismatch was 1.8 (1.1, 2.7; P = 0.01), and the risk associated with any HLA-DQB1 and/or HLA-DRB1 mismatch was 1.6 (1.2, 2.2; P = 0.003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_provenance.
- NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_assertion evidence source_evidence_literature NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_provenance.
- NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_assertion SIO_000772 8986816 NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_provenance.
- NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_assertion wasDerivedFrom befree-20140225 NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_provenance.
- NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_assertion wasGeneratedBy ECO_0000203 NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_provenance.
- befree-20140225 importedOn "2014-02-25" NP891072.RA7d0jSZ5IE6lVswK9mWWVFv4ApyYHWrRnr4cbrCUjwno130_provenance.