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- source_evidence_literature type ECO_0000212 NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_provenance.
- NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_assertion description "[The DNMT3A -448AG polymorphism is a novel functional SNP and contributes to its genetic susceptibility to GC. -448AG can be used as a stratification marker to predict an individuals susceptibility to GC, especially in the subgroups of individuals at the age range or= 60 years. However, the relative distribution of -448AG in EC can not be used as a prediction marker in order to evaluate an individuals susceptibility to EC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_provenance.
- NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_assertion evidence source_evidence_literature NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_provenance.
- NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_assertion SIO_000772 20128888 NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_provenance.
- NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_assertion wasDerivedFrom gad-20130706 NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_provenance.
- NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_assertion wasGeneratedBy ECO_0000203 NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_provenance.
- gad-20130706 importedOn "2013-07-06" NP88361.RAX9lwEN86-MsadHZUogi5QgoiW3qX9BYcG69PPYUun78130_provenance.