Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance.
- NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_assertion description "[The ALDH2 Lys and XRCC1 Gln variant alleles were associated with an increased risk of ESCC with adjusted ORs of 1.91 (95% CI, 0.96-3.80) and 1.67 (95% CI, 1.08-2.59), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance.
- NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_assertion evidence source_evidence_curated NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance.
- NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_assertion SIO_000772 16639733 NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance.
- NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_assertion wasDerivedFrom ctd_human-20130708 NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance.
- NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_assertion wasGeneratedBy ECO_0000218 NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance.