Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_provenance.
- NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_assertion description "[In contrast, 39% of the specimens showed APC methylation, which was more common in ADC (58%) than in SCC (13%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_provenance.
- NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_assertion evidence source_evidence_literature NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_provenance.
- NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_assertion SIO_000772 22542170 NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_provenance.
- NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_assertion wasDerivedFrom befree-20150227 NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_provenance.
- NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_assertion wasGeneratedBy ECO_0000203 NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP647856.RASQAxeLU0m3yEqEoVXRnFbwWJcgcOfvQGWXvDhEpHi5o130_provenance.