Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance.
- NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_assertion description "[The -93G>A (rs1800734) polymorphism located in the promoter of mismatch repair gene, MLH1, has been identified as a low-penetrance variant for cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance.
- NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_assertion evidence source_evidence_literature NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance.
- NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_assertion SIO_000772 23226285 NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance.
- NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_assertion wasDerivedFrom befree-20140225 NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance.
- NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_assertion wasGeneratedBy ECO_0000203 NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance.