Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_provenance.
- NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_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." NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_provenance.
- NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_assertion evidence source_evidence_literature NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_provenance.
- NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_assertion SIO_000772 9490271 NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_provenance.
- NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_assertion wasDerivedFrom befree-20150227 NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_provenance.
- NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_assertion wasGeneratedBy ECO_0000203 NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP240491.RAd9rg8Uw-4SKcuqzL2iCSVrA0oRwXeSVwnIBAgHpmcTE130_provenance.