Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance.
- befree-2016 importedOn "2016-02-19" NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance.
- NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_assertion wasGeneratedBy ECO_0000203 NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance.
- NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_assertion wasDerivedFrom befree-2016 NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance.
- NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_assertion SIO_000772 10399872 NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance.
- NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_assertion evidence source_evidence_literature NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance.
- NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance.