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- source_evidence_literature type ECO_0000212 NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_provenance.
- NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_assertion description "[Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant, late-onset neurodegenerative disease caused by a polyglutamine (polyQ) expansion in the ataxin-1 protein, which causes progressive neurodegeneration in cerebellar Purkinje cells and brainstem nuclei.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_provenance.
- NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_assertion evidence source_evidence_literature NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_provenance.
- NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_assertion SIO_000772 24419082 NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_provenance.
- NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_assertion wasDerivedFrom befree-20150227 NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_provenance.
- NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_assertion wasGeneratedBy ECO_0000203 NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_provenance.