Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_provenance.
- NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_assertion description "[Patients with N1M0 and N0M1 disease demonstrated significant differences in 5-year DSS: 74% versus 14% at MDACC (P = .014) and 52% versus 0% in SEER (P = .014).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_provenance.
- NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_assertion evidence source_evidence_literature NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_provenance.
- NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_assertion SIO_000772 19402173 NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_provenance.
- NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_assertion wasDerivedFrom befree-20140225 NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_provenance.
- NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_assertion wasGeneratedBy ECO_0000203 NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP245033.RAcX6SJGChecBuwWDeqdYNNmt5A8NxJzB7nwMGBGLNnuM130_provenance.