Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_provenance.
- NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_assertion description "[This produced an early-onset clinical syndrome that combines the severe phenotypes of SPG7 and SCA28, in additional to other `mitochondrial` features such as oculomotor apraxia, extrapyramidal dysfunction, and myoclonic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_provenance.
- NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_assertion evidence source_evidence_literature NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_provenance.
- NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_assertion SIO_000772 22022284 NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_provenance.
- NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_assertion wasDerivedFrom befree-20140225 NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_provenance.
- NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_assertion wasGeneratedBy ECO_0000203 NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP328480.RAud3O8O72REhEaQaFCofcnn8inKqm78KWd0okpJ_dImw130_provenance.