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- source_evidence_literature type ECO_0000212 NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_provenance.
- NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_assertion description "[However, allele sizes within the SCA8 proposed pathogenic range have been reported in patients with ataxia of unknown etiology, in individuals from pedigrees with other SCA or Friedreich's ataxia, and in patients with Alzheimer's disease, schizophrenia or parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_provenance.
- NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_assertion evidence source_evidence_literature NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_provenance.
- NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_assertion SIO_000772 18708037 NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_provenance.
- NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_assertion wasDerivedFrom befree-2016 NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_provenance.
- NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_assertion wasGeneratedBy ECO_0000203 NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_provenance.
- befree-2016 importedOn "2016-02-19" NP688093.RAEvmkuJWXsolIljfByNAFiC40cDeC2mB29yTD-64Bz6M130_provenance.