Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_provenance.
- NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_assertion description "[However, future observations of paroxsymal ataxia and, possibly, areflexia in other DARS2-mutated patients are warranted to further corroborate our finding that DARS2 mutations can lead to a paroxsymal ataxia phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_provenance.
- NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_assertion evidence source_evidence_literature NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_provenance.
- NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_assertion SIO_000772 21749991 NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_provenance.
- NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_assertion wasDerivedFrom befree-2016 NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_provenance.
- NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_assertion wasGeneratedBy ECO_0000203 NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_provenance.
- befree-2016 importedOn "2016-02-19" NP909075.RAZBirV9ctmg-uxqq6yoOUUVAXzMVB4u-PsYfg0AmT4T0130_provenance.