Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_assertion> ?p ?o ?g. }
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- NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_assertion type Assertion NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_head.
- NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_assertion wasGeneratedBy ECO_0000203 NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_provenance.
- NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_assertion wasDerivedFrom befree-2016 NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_provenance.
- NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_assertion SIO_000772 18285829 NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_provenance.
- NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_assertion evidence source_evidence_literature NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_provenance.
- NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_assertion description "[Spinocerebellar ataxia type 6 (SCA6) is a common cause of dominantly inherited ataxia due to an expansion of the CAG repeat in the CACNA1A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656326.RAITViT0AlOW11lgDzQwObGvJjF2WlemMQCDnrFiVnQ54130_provenance.