Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_assertion type Assertion NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_head.
- NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_assertion description "[The GGGGCC hexanucleotide expansion in the C9ORF72 gene is the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_provenance.
- NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_assertion evidence source_evidence_literature NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_provenance.
- NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_assertion SIO_000772 25467142 NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_provenance.
- NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_assertion wasDerivedFrom befree-2016 NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_provenance.
- NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_assertion wasGeneratedBy ECO_0000203 NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_provenance.