Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_provenance.
- NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_assertion description "[EGF genotyping can potentially identify high-risk patients with GERD and Barrett's metaplasia who might benefit from increased surveillance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_provenance.
- NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_assertion evidence source_evidence_literature NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_provenance.
- NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_assertion SIO_000772 18483390 NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_provenance.
- NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_assertion wasDerivedFrom gad-20150221 NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_provenance.
- NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_assertion wasGeneratedBy ECO_0000203 NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_provenance.
- gad-20150221 importedOn "2015-02-21" NP109751.RAwUGDRJNNV_uUhJgHW5A-dGXGyQV2y2e6iBmiFxXHc3w130_provenance.