Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance.
- NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance.
- NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_assertion evidence source_evidence_literature NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance.
- NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_assertion SIO_000772 20137776 NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance.
- NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_assertion wasDerivedFrom befree-2016 NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance.
- NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_assertion wasGeneratedBy ECO_0000203 NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance.
- befree-2016 importedOn "2016-02-19" NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance.