Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_provenance.
- NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_assertion description "[Copy number losses in early BE were observed at particularly high frequency at FRA3B (81%), FRA9A/C (71.4%), FRA5E (52.4%), and FRA 4D (52.4%), and at lower frequencies in other fragile sites, including FRA1K (42.9%), FRAXC (42.9%), FRA 12B (33.3%), and FRA16D (33.3%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_provenance.
- NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_assertion evidence source_evidence_literature NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_provenance.
- NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_assertion SIO_000772 20647332 NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_provenance.
- NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_assertion wasDerivedFrom befree-20140225 NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_provenance.
- NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_assertion wasGeneratedBy ECO_0000203 NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP486539.RAIIm1ozHouVhSoxrakrVMCxAuNxRIR2xJ5lEPMD8vUlg130_provenance.