Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_provenance.
- NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_assertion description "[The subjects included 734 patients with SCA (480 patients with sporadic SCA and 254 patients with familial SCA) without CAG repeat expansions at the SCA1, SCA2, Machado-Joseph disease, SCA6, SCA7, or dentatorubral-pallidolluysian atrophy loci, with 162 healthy subjects, 216 patients with Parkinson disease, and 195 with Alzheimer disease as control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_provenance.
- NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_assertion evidence source_evidence_literature NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_provenance.
- NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_assertion SIO_000772 14967767 NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_provenance.
- NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_assertion wasDerivedFrom befree-2016 NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_provenance.
- NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_assertion wasGeneratedBy ECO_0000203 NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_provenance.
- befree-2016 importedOn "2016-02-19" NP431998.RAkoByCL20BkQf26TMB0ebFLylgS9bxW3r9qjdAEahrd0130_provenance.