Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_assertion> ?p ?o ?g. }
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- NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_assertion type Assertion NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_head.
- NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_assertion description "[Heterozygous mutations in GRN are a major cause of frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP), the second most common early-onset dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_provenance.
- NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_assertion evidence source_evidence_literature NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_provenance.
- NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_assertion SIO_000772 22608501 NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_provenance.
- NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_assertion wasDerivedFrom befree-20140225 NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_provenance.
- NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_assertion wasGeneratedBy ECO_0000203 NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_provenance.