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- source_evidence_literature type ECO_0000212 NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_provenance.
- NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_assertion description "[The DNMT3A -448A>G polymorphism is a novel functional SNP and contributes to its genetic susceptibility to GC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_provenance.
- NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_assertion evidence source_evidence_literature NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_provenance.
- NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_assertion SIO_000772 20128888 NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_provenance.
- NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_assertion wasDerivedFrom befree-2016 NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_provenance.
- NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_assertion wasGeneratedBy ECO_0000203 NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_provenance.
- befree-2016 importedOn "2016-02-19" NP791581.RA9YZGgHLS8NvSVTIwyANtX0G-LQW9Z7ONHhczhCDQBks130_provenance.