Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_assertion> ?p ?o ?g. }
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- NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_assertion type Assertion NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_head.
- NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_assertion wasGeneratedBy ECO_0000203 NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_provenance.
- NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_assertion wasDerivedFrom befree-2016 NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_provenance.
- NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_assertion SIO_000772 24119542 NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_provenance.
- NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_assertion evidence source_evidence_literature NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_provenance.
- NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_assertion description "[Our data corroborate and extend previous findings to include an increased frequency of rare heterozygous TREM2 variations in AD and FTD, and show that TREM2 variants may play a role in neurodegenerative diseases in general.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1118452.RA5zisNbcu8lV7SvNqqs8DC8Yt71b5YRDLX7j-tS6uaU0130_provenance.