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- NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_assertion type Assertion NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_head.
- NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_assertion wasGeneratedBy ECO_0000203 NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_provenance.
- NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_assertion wasDerivedFrom gad-20150221 NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_provenance.
- NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_assertion SIO_000772 17440947 NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_provenance.
- NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_assertion evidence source_evidence_literature NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_provenance.
- NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_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." NP106895.RAwvljq66HPcIoi47iI-5IZiUlSGc0PrwBe6cQD9nBLYw130_provenance.