Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_provenance.
- NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_assertion description "[Uni- and multivariable analyses for recurrence and progression were performed using clinicopathological variables, T1 sub-stage, EORTC risk scores and molecular markers (fibroblast growth factor receptor 3 gene mutation and Ki-67, P53, P27 expression).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_provenance.
- NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_assertion evidence source_evidence_literature NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_provenance.
- NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_assertion SIO_000772 22448597 NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_provenance.
- NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_assertion wasDerivedFrom befree-20140225 NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_provenance.
- NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_assertion wasGeneratedBy ECO_0000203 NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP452890.RAdvM-fvFovkKPQxCZEDEWlCYRBZHuTTUgbK0JhwJndBw130_provenance.