Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP318403.RAAo2Qb7WnKn88MHxVeFyRmSrZ9AJWIJpmDMR-TVWbAZo130_provenance.