Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_assertion> ?p ?o ?g. }
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- NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_assertion type Assertion NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_head.
- NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_assertion description "[The most common cause of inherited SCA was a mutation at the SCA6 locus (25%), followed by mutation at the SCA1 locus (15%), SCA3 locus (5%) and dentatorubral-pallidoluysian atrophy locus (5%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_provenance.
- NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_assertion evidence source_evidence_literature NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_provenance.
- NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_assertion SIO_000772 11359084 NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_provenance.
- NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_assertion wasDerivedFrom befree-2016 NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_provenance.
- NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_assertion wasGeneratedBy ECO_0000203 NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_provenance.