Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_assertion> ?p ?o ?g. }
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- NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_assertion type Assertion NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_head.
- NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_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." NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_provenance.
- NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_assertion evidence source_evidence_literature NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_provenance.
- NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_assertion SIO_000772 21749991 NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_provenance.
- NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_assertion wasDerivedFrom befree-20140225 NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_provenance.
- NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_assertion wasGeneratedBy ECO_0000203 NP336241.RAQlxi6c9HnO2xKUvnpMhURIUd_YOed5QQTGZNHGKeleM130_provenance.