Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_assertion> ?p ?o ?g. }
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- NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_assertion type Assertion NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_head.
- NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_assertion wasGeneratedBy ECO_0000203 NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_provenance.
- NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_assertion wasDerivedFrom befree-20140225 NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_provenance.
- NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_assertion SIO_000772 17030535 NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_provenance.
- NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_assertion evidence source_evidence_literature NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_provenance.
- NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_assertion description "[These findings suggest that the insR352 PSEN1 is not pathogenic, and the IVS1+1G-->A mutation in PGRN causes FTDP associated with FTLD-U pathology and represents a new class of neurodegenerative disease--the 'hypoprogranulinopathies'.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623175.RA89JWXy1aG74I4bsLSsqgq1FRKNDXgY4MJIFIte1uIoY130_provenance.