Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_assertion> ?p ?o ?g. }
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- NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_assertion type Assertion NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_head.
- NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_assertion description "[Hexanucleotide repeat expansions in chromosome 9 open reading frame 72 (C9ORF72) are the most common known genetic cause of frontotemporal dementia (FTD) and motor neuron disease (MND).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_provenance.
- NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_assertion evidence source_evidence_literature NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_provenance.
- NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_assertion SIO_000772 24011653 NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_provenance.
- NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_assertion wasDerivedFrom befree-2016 NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_provenance.
- NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_assertion wasGeneratedBy ECO_0000203 NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_provenance.