Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_assertion> ?p ?o ?g. }
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- NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_assertion type Assertion NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_head.
- NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_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." NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_provenance.
- NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_assertion evidence source_evidence_literature NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_provenance.
- NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_assertion SIO_000772 9490271 NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_provenance.
- NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_assertion wasDerivedFrom befree-2016 NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_provenance.
- NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_assertion wasGeneratedBy ECO_0000203 NP1389912.RAntPtOhNhtMkBMryKO2eABvqPRcABKu0YFl8W7ouPwcE130_provenance.