Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_provenance.
- NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_assertion description "[The aim of the present study was to examine the association between the L757P polymorphism at exon 13 of the EXO1 gene and the risk of CRC in Iranian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_provenance.
- NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_assertion evidence source_evidence_literature NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_provenance.
- NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_assertion SIO_000772 20854105 NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_provenance.
- NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_assertion wasDerivedFrom befree-20140225 NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_provenance.
- NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_assertion wasGeneratedBy ECO_0000203 NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP188668.RA6p-gnaYSdXsmdaX8VlCHnrTsZ9VhMdYRNSMKijt-KcM130_provenance.