Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_provenance.
- NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_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." NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_provenance.
- NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_assertion evidence source_evidence_literature NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_provenance.
- NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_assertion SIO_000772 9490271 NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_provenance.
- NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_assertion wasDerivedFrom befree-20140225 NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_provenance.
- NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_assertion wasGeneratedBy ECO_0000203 NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP327083.RArWUjz1DwWsNLU3R0fiM6hkCe0-R8Y38a9giT424WprI130_provenance.