Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_provenance.
- NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_assertion description "[Finally, comparing our results with the findings from other European populations, the LRP1 C allele frequency showed a statistically significant decreasing trend from Northern to Southern regions of Europe, with a concomitant increase in LRP1 T allele frequency, but in AD patients only.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_provenance.
- NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_assertion evidence source_evidence_literature NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_provenance.
- NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_assertion SIO_000772 15048651 NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_provenance.
- NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_assertion wasDerivedFrom gad-20150221 NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_provenance.
- NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_assertion wasGeneratedBy ECO_0000203 NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP69483.RAbSXZJxG5-8WkuvhzSITLMFH_3TmaAv1ClL3JQ37nDZM130_provenance.