Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_assertion> ?p ?o ?g. }
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- NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_assertion type Assertion NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_head.
- NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_assertion description "[The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of sporadic and familial forms of amyotrophic lateral sclerosis and frontotemporal dementia.The basis for pathogenesis is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_provenance.
- NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_assertion evidence source_evidence_literature NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_provenance.
- NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_assertion SIO_000772 26308899 NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_provenance.
- NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_assertion wasDerivedFrom befree-2016 NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_provenance.
- NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_assertion wasGeneratedBy ECO_0000203 NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_provenance.