Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance.
- NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_assertion wasGeneratedBy ECO_0000203 NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance.
- NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_assertion wasDerivedFrom gad-20130706 NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance.
- NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_assertion SIO_000772 17440947 NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance.
- NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_assertion evidence source_evidence_literature NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance.
- NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_assertion description "[Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance.