Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_assertion> ?p ?o ?g. }
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- NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_assertion type Assertion NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_head.
- NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_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." NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_provenance.
- NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_assertion evidence source_evidence_literature NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_provenance.
- NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_assertion SIO_000772 25467142 NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_provenance.
- NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_assertion wasDerivedFrom befree-2016 NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_provenance.
- NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_assertion wasGeneratedBy ECO_0000203 NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_provenance.