Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_provenance.
- NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_assertion description "[GSTM1-null genotype or combination of the GSTM1-null and GSTT1-positive genotypes in females may be associated with increased risk of cataract development in the Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_provenance.
- NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_assertion evidence source_evidence_literature NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_provenance.
- NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_assertion SIO_000772 17514530 NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_provenance.
- NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_assertion wasDerivedFrom befree-20140225 NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_provenance.
- NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_assertion wasGeneratedBy ECO_0000203 NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP284291.RAiB_IFrVmpePRTVsJGFV6eoEV5sTB2VnvkE24hRn7Q8E130_provenance.