Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance.