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- source_evidence_literature type ECO_0000212 NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_provenance.
- NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_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." NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_provenance.
- NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_assertion evidence source_evidence_literature NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_provenance.
- NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_assertion SIO_000772 22300873 NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_provenance.
- NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_assertion wasDerivedFrom befree-2016 NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_provenance.
- NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_assertion wasGeneratedBy ECO_0000203 NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_provenance.
- befree-2016 importedOn "2016-02-19" NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_provenance.