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- source_evidence_literature type ECO_0000212 NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance.
- NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_assertion description "[Genotypes were available for 40 SNPs across the ADH genes cluster and 24 SNPs across the two ALDH genes in four diverse samples that included cases (lifetime AD) and controls (no Axis 1 disorders).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance.
- NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_assertion evidence source_evidence_literature NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance.
- NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_assertion SIO_000772 21083667 NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance.
- NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_assertion wasDerivedFrom befree-2016 NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance.
- NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_assertion wasGeneratedBy ECO_0000203 NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance.
- befree-2016 importedOn "2016-02-19" NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance.