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- source_evidence_literature type ECO_0000212 NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_provenance.
- NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_assertion description "[Results were similar when the analysis was restricted to MDS and CMML patients, excluding AML (HR=2.46 (95% confidence interval: 1.1-6.4); p=0.04)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_provenance.
- NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_assertion evidence source_evidence_literature NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_provenance.
- NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_assertion SIO_000772 24836762 NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_provenance.
- NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_assertion wasDerivedFrom befree-2016 NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_provenance.
- NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_assertion wasGeneratedBy ECO_0000203 NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1183167.RAnQV1702LymzP2EiLCLhbgurI_wBBMRRArgMs6QLQySg130_provenance.