Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_provenance.
- NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_assertion description "[By using primary esophageal tissue samples we determined that PKP1 was rarely methylated in normal squamous esophagus (5/55; 9.1%) and BE (5/39; 12.8%) and more frequently methylated in Barrett's esophagus with high-grade dysplasia (HGD) or EAC (20/60; 33.3%; P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_provenance.
- NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_assertion evidence source_evidence_literature NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_provenance.
- NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_assertion SIO_000772 22170739 NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_provenance.
- NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_assertion wasDerivedFrom befree-20140225 NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_provenance.
- NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_assertion wasGeneratedBy ECO_0000203 NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP421050.RAHcZF22uij1BGyEnHp_1ragFbFREwqhTD7Z86dNNSZg4130_provenance.