Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_provenance.
- NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_assertion description "[The low frequency of LOH in the p16 gene (9p) in adenomas compared with dysplasia in UC combined with infrequent LOH in APC gene loci in cases of pure dysplasia in UC may support this combination of markers as a clinical test for the differentiation of polypoid dysplasia from adenomas in UC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_provenance.
- NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_assertion evidence source_evidence_literature NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_provenance.
- NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_assertion SIO_000772 9490271 NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_provenance.
- NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_assertion wasDerivedFrom befree-20150227 NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_provenance.
- NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_assertion wasGeneratedBy ECO_0000203 NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP304456.RARzXAWkEIsc6Hx9xrzZuw5DXAXJApuOPlYzSETjEdz_M130_provenance.