Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_assertion> ?p ?o ?g. }
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- NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_assertion type Assertion NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_head.
- NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_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." NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_provenance.
- NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_assertion evidence source_evidence_literature NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_provenance.
- NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_assertion SIO_000772 22022284 NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_provenance.
- NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_assertion wasDerivedFrom befree-20150227 NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_provenance.
- NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_assertion wasGeneratedBy ECO_0000203 NP856478.RAGSnf249ZxiXH0y5xJoc1LogxWEkH1Ewc68e2ksg79BE130_provenance.