Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_provenance.
- NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_assertion description "[There was no difference in frequencies of high-level CpG island methylation (CIM-H, methylation index > or =0.5) among flat dysplasias (50%) and polypoid adenomas (51%) unassociated with carcinoma, dysplasias/adenomas associated with adenocarcinoma (47%), and adenocarcinoma (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_provenance.
- NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_assertion evidence source_evidence_literature NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_provenance.
- NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_assertion SIO_000772 15064707 NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_provenance.
- NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_assertion wasDerivedFrom befree-20140225 NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_provenance.
- NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_assertion wasGeneratedBy ECO_0000203 NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP201023.RA83AS_zrn1U7R9-4DOkcBtabWFFxn2nGxfMi6CCr31vA130_provenance.