Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_assertion> ?p ?o ?g. }
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- NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_assertion type Assertion NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_head.
- NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_assertion description "[Recently, 2 independent studies reported that a rare missense variant, rs75932628 (R47H), in exon 2 of the gene encoding the triggering receptor expressed on myeloid cells 2 (TREM2) significantly increases the risk of Alzheimer disease (AD) with an effect size comparable to that of the APOE ?4 allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_provenance.
- NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_assertion evidence source_evidence_literature NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_provenance.
- NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_assertion SIO_000772 25186855 NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_provenance.
- NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_assertion wasDerivedFrom befree-2016 NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_provenance.
- NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_assertion wasGeneratedBy ECO_0000203 NP1216612.RALuzoTCHY9MtvvLTro9QWggB0H5PTiygfKEKhCI7G7JA130_provenance.