Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_provenance.
- NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_assertion description "[In the cases of CLU, PICALM and CR1, as well as in APOE, the odds ratios we find are slightly larger than those previously reported in clinical samples, consistent with what we believe to be more accurate classification of disease in the clinically characterized and neuropathologically confirmed AD cases and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_provenance.
- NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_assertion evidence source_evidence_literature NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_provenance.
- NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_assertion SIO_000772 20534741 NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_provenance.
- NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_assertion wasDerivedFrom befree-20140225 NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_provenance.
- NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_assertion wasGeneratedBy ECO_0000203 NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_provenance.
- befree-20140225 importedOn "2014-02-25" NP209374.RA-lllGSc5xa_sKlPpqcxgXN-EJd_Buchnlzk87rrNvro130_provenance.