Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_provenance.
- NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_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." NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_provenance.
- NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_assertion evidence source_evidence_literature NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_provenance.
- NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_assertion SIO_000772 22270878 NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_provenance.
- NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_assertion wasDerivedFrom befree-20140225 NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_provenance.
- NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_assertion wasGeneratedBy ECO_0000203 NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP241166.RAH1lWu417L9AZXoWL_EHyHObjdTOfIO3b6dd1mJlVQMI130_provenance.