Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_assertion type Assertion NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_head.
- NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_assertion description "[A GGGGCC-repeat expansion in C9orf72 is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) among Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_provenance.
- NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_assertion evidence source_evidence_literature NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_provenance.
- NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_assertion SIO_000772 25712133 NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_provenance.
- NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_assertion wasDerivedFrom befree-2016 NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_provenance.
- NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_assertion wasGeneratedBy ECO_0000203 NP1266026.RAbzHOdlGi3_KOI7wOodLK4kcTTtxLvmjQv4_lLizgUns130_provenance.