Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_provenance.
- NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_assertion description "[Our observations do not support a role for common POLG1 genetic variants in PD and indicate that dominant POLG1 mutations are a rare cause of parkinsonism in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_provenance.
- NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_assertion evidence source_evidence_literature NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_provenance.
- NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_assertion SIO_000772 16943369 NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_provenance.
- NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_assertion wasDerivedFrom lhgdn-20090331 NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_provenance.
- NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_assertion wasGeneratedBy ECO_0000203 NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_provenance.