Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_provenance.
- NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_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." NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_provenance.
- NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_assertion evidence source_evidence_literature NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_provenance.
- NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_assertion SIO_000772 22022284 NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_provenance.
- NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_assertion wasDerivedFrom befree-2016 NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_provenance.
- NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_assertion wasGeneratedBy ECO_0000203 NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_provenance.
- befree-2016 importedOn "2016-02-19" NP933167.RAiIrQCxs9gTF_oqsE_zH4hyEdJo-iXl3xsE5zjZBGeWA130_provenance.