Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_assertion> ?p ?o ?g. }
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- NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_assertion type Assertion NP111000.RAjEcOoItI_TH8LhOTeVH62Tg5KHiJjgF8U4aiVnAwqCo130_head.
- 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.