Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_provenance.
- NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_assertion description "[Statistically significant association between genotype at 7p12.2 (IKZF1), 10q21.2 (ARID5B) and the NBS associated locus, 8q21.3 (NBN) and ALL risk was found; odds ratios (ORs), 1.34 (P=0.002), 1.33 (P=0.003), and 1325.21 (P=0.0028), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_provenance.
- NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_assertion evidence source_evidence_literature NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_provenance.
- NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_assertion SIO_000772 21889209 NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_provenance.
- NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_assertion wasDerivedFrom befree-20140225 NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_provenance.
- NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_assertion wasGeneratedBy ECO_0000203 NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478772.RATXvAULHWS6At3STPKYnJJhKv43i8mo8b7RnoY9E9-Xg130_provenance.