Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_provenance.
- NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_assertion description "[The linkage between mutations and clinical and pathologic outcomes was interrogated with the Fisher exact test (for stage and Fuhrman nuclear grade) and the permutation log-rank test (for cancer-specific survival [CSS]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_provenance.
- NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_assertion evidence source_evidence_literature NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_provenance.
- NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_assertion SIO_000772 23036577 NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_provenance.
- NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_assertion wasDerivedFrom befree-20150227 NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_provenance.
- NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_assertion wasGeneratedBy ECO_0000203 NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP922008.RAc53lFcEF2bt62RJn9xoiRB33Rhz_NOjnBi9sGlhV05I130_provenance.