Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_assertion> ?p ?o ?g. }
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- NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_assertion type Assertion NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_head.
- NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_assertion wasGeneratedBy ECO_0000203 NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_provenance.
- NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_assertion wasDerivedFrom gad-20150221 NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_provenance.
- NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_assertion SIO_000772 17440947 NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_provenance.
- NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_assertion evidence source_evidence_literature NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_provenance.
- NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_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." NP58210.RAIPbNS3RJhxn_uP5_z6B9kUoWpcsxoftTOB-awZqJox8130_provenance.