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- source_evidence_literature type ECO_0000212 NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_provenance.
- NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_assertion description "[These results were further supported by the CART analysis which revealed that individuals with the combined genotypes of ESR1-397 CT or TT, ESR1-351 AG or GG and ESR2 -789 AA had the highest risk for GBC [OR = 3.9].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_provenance.
- NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_assertion evidence source_evidence_literature NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_provenance.
- NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_assertion SIO_000772 22808109 NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_provenance.
- NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_assertion wasDerivedFrom befree-2016 NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_provenance.
- NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_assertion wasGeneratedBy ECO_0000203 NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_provenance.
- befree-2016 importedOn "2016-02-19" NP998431.RASaJn-ZSI-Ntsh-zInlDtEtev5yNk3p9-XpmF_dfWEeA130_provenance.