Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_provenance.
- NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_assertion description "[BRAF mutation was mainly detected in SSA/P with dysplasia (95%), SSA/P (85%), microvesicular HP (76%), and traditional serrated adenoma (54%), whereas KRAS mutation was present mainly in goblet cell HP (50%) and in tubulovillous adenoma (45%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_provenance.
- NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_assertion evidence source_evidence_literature NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_provenance.
- NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_assertion SIO_000772 22510757 NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_provenance.
- NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_assertion wasDerivedFrom befree-20150227 NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_provenance.
- NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_assertion wasGeneratedBy ECO_0000203 NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP528045.RAI9h8OvrS1ZBAoGl-Sn3yxgg-LTVe_8pbWrS0V8wBA4A130_provenance.