Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_assertion> ?p ?o ?g. }
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- NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_assertion type Assertion NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_head.
- NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_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." NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_provenance.
- NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_assertion evidence source_evidence_literature NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_provenance.
- NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_assertion SIO_000772 9490271 NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_provenance.
- NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_assertion wasDerivedFrom befree-2016 NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_provenance.
- NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_assertion wasGeneratedBy ECO_0000203 NP1389907.RAtwekLYW2kVTo3bVooOVDGsSfAQWE25KzTt7QQ9jLl8M130_provenance.