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- source_evidence_literature type ECO_0000212 NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_provenance.
- NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_assertion description "[Predisposition to cancer in this syndrome results from increased accumulation of mutations due to defective mismatch repair (MMR) caused by a mutation in one of the mismatch repair genes MLH1, MSH2, MSH6 or PMS2/scPMS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_provenance.
- NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_assertion evidence source_evidence_literature NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_provenance.
- NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_assertion SIO_000772 24204293 NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_provenance.
- NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_assertion wasDerivedFrom befree-20150227 NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_provenance.
- NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_assertion wasGeneratedBy ECO_0000203 NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP569676.RADIELXw0X2em5l917ksKkuryv87eGIuW935aI9GKzYQM130_provenance.