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- source_evidence_literature type ECO_0000212 NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_provenance.
- NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_assertion description "[Here we report a secondary reduction in calpain 3 expression in eight out of 16 patients with a primary dysferlinopathy and clinical features characteristic of limb girdle muscular dystrophy type 2B or Miyoshi myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_provenance.
- NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_assertion evidence source_evidence_literature NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_provenance.
- NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_assertion SIO_000772 11053681 NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_provenance.
- NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_assertion wasDerivedFrom befree-20140225 NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_provenance.
- NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_assertion wasGeneratedBy ECO_0000203 NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP167515.RAVuZ_FfDsG-qWi_Kduao9lNOT3hEjfYj-6XVj5P2xUw0130_provenance.