Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_provenance.
- NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_assertion description "[We included patients suffering from Friedreich's ataxia (FRDA, n = 83), early onset cerebellar ataxia (EOCA, n = 30), autosomal dominant cerebellar ataxia (ADCA) type I (ADCA-I, n = 273), ADCA-III (n = 13) and multiple system atrophy (MSA, n = 67).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_provenance.
- NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_assertion evidence source_evidence_literature NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_provenance.
- NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_assertion SIO_000772 9577387 NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_provenance.
- NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_assertion wasDerivedFrom befree-20140225 NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_provenance.
- NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_assertion wasGeneratedBy ECO_0000203 NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP719239.RAhRX6q4uJXum1eggy0bLfDmoRq4w6buMvB_MMqm4Cixs130_provenance.