Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_provenance.
- NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_assertion description "[We studied the frequencies of polymorphic variants in CYP1A1, GSTP1, GSTT1, and GSTM1 genes in 98 patients with Barrett's epithelium and 34 patients with esophageal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_provenance.
- NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_assertion evidence source_evidence_literature NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_provenance.
- NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_assertion SIO_000772 9973204 NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_provenance.
- NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_assertion wasDerivedFrom befree-2016 NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_provenance.
- NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_assertion wasGeneratedBy ECO_0000203 NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1414524.RAu6K-2gn9i6vlZ9Ji4ZlrYy6vZENY7P2BFRZPAaa0hcg130_provenance.