Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_assertion> ?p ?o ?g. }
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- NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_assertion type Assertion NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_head.
- NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_assertion description "[We investigated the relative prevalence of SCA1-3, 6-8, 12, 17; dentate-rubro-pallidoluysian atrophy; and Friedreich's ataxia (FRDA) in Serbian patients with adult-onset (>20 years of age) hereditary and sporadic SCAs, and compared clinical features of patients with genetically confirmed SCAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_provenance.
- NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_assertion evidence source_evidence_literature NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_provenance.
- NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_assertion SIO_000772 16149098 NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_provenance.
- NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_assertion wasDerivedFrom befree-20150227 NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_provenance.
- NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_assertion wasGeneratedBy ECO_0000203 NP681553.RAHWJn1RQcyrdel7d7q3GTJLb1s9uuTvWyhQN-RPQIpBs130_provenance.