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- NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_assertion type Assertion NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_head.
- 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.