Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_assertion> ?p ?o ?g. }
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- NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_assertion type Assertion NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_head.
- NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_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." NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_provenance.
- NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_assertion evidence source_evidence_literature NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_provenance.
- NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_assertion SIO_000772 22022284 NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_provenance.
- NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_assertion wasDerivedFrom befree-20140225 NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_provenance.
- NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_assertion wasGeneratedBy ECO_0000203 NP763736.RAmUlat8hJJZuHhpXj-1XITvZhvjH24RnVgVDoDZJsjMY130_provenance.