Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_provenance.
- NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_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." NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_provenance.
- NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_assertion evidence source_evidence_literature NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_provenance.
- NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_assertion SIO_000772 22448597 NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_provenance.
- NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_assertion wasDerivedFrom befree-20150227 NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_provenance.
- NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_assertion wasGeneratedBy ECO_0000203 NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP851125.RAWQkA4SIhrtJlXXqFiE-WB5h7LSEkHAgcjN7SFxWQwX0130_provenance.