Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_provenance.
- NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_assertion description "[The patient presented with myoclonic epilepsy beginning at 10�years of age, a muscle biopsy with ragged red fibres and some COX negative fibres and progressive bilateral MRI hyperintensitivities in the basal ganglia constituting MERRF syndrome but lacked clinical characteristics of MELAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_provenance.
- NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_assertion evidence source_evidence_literature NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_provenance.
- NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_assertion SIO_000772 22270878 NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_provenance.
- NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_assertion wasDerivedFrom befree-20140225 NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_provenance.
- NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_assertion wasGeneratedBy ECO_0000203 NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP495036.RA3FUqgwYw-wdZBOzVN6teqIs2bwWOns0VTxgyBh2F3C0130_provenance.