Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_provenance.
- NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_assertion description "[We suggest that SCA6, in common with SCA2 and SCA3, may be associated with Parkinsonism attributable to nigral loss and dopaminergic dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_provenance.
- NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_assertion evidence source_evidence_literature NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_provenance.
- NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_assertion SIO_000772 15954136 NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_provenance.
- NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_assertion wasDerivedFrom befree-2016 NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_provenance.
- NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_assertion wasGeneratedBy ECO_0000203 NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_provenance.
- befree-2016 importedOn "2016-02-19" NP499322.RAGs5xB0lIXnZ19e-osfUoEZ4B3RWnpWr5MpLwuqLMQbc130_provenance.