Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_assertion> ?p ?o ?g. }
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- NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_assertion type Assertion NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_head.
- NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_assertion description "[The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as the cause of chromosome 9-linked frontotemporal dementia and motor neuron disease offers the opportunity for greater understanding of the relationship between these disorders and other clinical forms of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance.
- NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_assertion evidence source_evidence_literature NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance.
- NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_assertion SIO_000772 22300873 NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance.
- NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_assertion wasDerivedFrom befree-20140225 NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance.
- NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_assertion wasGeneratedBy ECO_0000203 NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance.