Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_provenance.
- NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_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." NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_provenance.
- NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_assertion evidence source_evidence_literature NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_provenance.
- NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_assertion SIO_000772 9490271 NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_provenance.
- NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_assertion wasDerivedFrom befree-2016 NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_provenance.
- NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_assertion wasGeneratedBy ECO_0000203 NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1389908.RAtpUUXUCSsCBZ6cNSywjBLDJHX7n3Dx4Xy5VX3nSS7fE130_provenance.