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- source_evidence_literature type ECO_0000212 NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_provenance.
- NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_assertion description "[SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_provenance.
- NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_assertion evidence source_evidence_literature NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_provenance.
- NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_assertion SIO_000772 24042580 NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_provenance.
- NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_assertion wasDerivedFrom befree-20150227 NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_provenance.
- NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_assertion wasGeneratedBy ECO_0000203 NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_provenance.
- befree-20150227 importedOn "2015-02-27" NP810187.RAu6tn47CXQWxj3hF78dOwGuspaKXlBiN2ZG7mvQCSfno130_provenance.