Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_assertion> ?p ?o ?g. }
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- NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_assertion type Assertion NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_head.
- NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_assertion description "[These data provide both the first genetic evidence and functional studies supporting the role of MAPT p.A152T as a rare risk factor for both FTD-s and AD and the concept that rare variants can increase the risk for relatively common, complex neurodegenerative diseases, but since no clear significance threshold for rare genetic variation has been established, some caution is warranted until the findings are further replicated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_provenance.
- NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_assertion evidence source_evidence_literature NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_provenance.
- NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_assertion SIO_000772 22556362 NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_provenance.
- NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_assertion wasDerivedFrom befree-2016 NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_provenance.
- NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_assertion wasGeneratedBy ECO_0000203 NP979612.RAroWDNnWeZxM_ZN0fBvSUXVqy02O08RNVvsx4_Rqgnqs130_provenance.