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- NP362710.RADtsOL4FC3SpyxB9ulzDKfGqwDIf9fFU0jbEZ1YN2ok8130_assertion type Assertion NP362710.RADtsOL4FC3SpyxB9ulzDKfGqwDIf9fFU0jbEZ1YN2ok8130_head.
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- NP362710.RADtsOL4FC3SpyxB9ulzDKfGqwDIf9fFU0jbEZ1YN2ok8130_assertion wasDerivedFrom befree-20150227 NP362710.RADtsOL4FC3SpyxB9ulzDKfGqwDIf9fFU0jbEZ1YN2ok8130_provenance.
- NP362710.RADtsOL4FC3SpyxB9ulzDKfGqwDIf9fFU0jbEZ1YN2ok8130_assertion SIO_000772 11555628 NP362710.RADtsOL4FC3SpyxB9ulzDKfGqwDIf9fFU0jbEZ1YN2ok8130_provenance.
- NP362710.RADtsOL4FC3SpyxB9ulzDKfGqwDIf9fFU0jbEZ1YN2ok8130_assertion evidence source_evidence_literature NP362710.RADtsOL4FC3SpyxB9ulzDKfGqwDIf9fFU0jbEZ1YN2ok8130_provenance.
- NP362710.RADtsOL4FC3SpyxB9ulzDKfGqwDIf9fFU0jbEZ1YN2ok8130_assertion description "[These alterations are comparable with those found in the partial trisomy chromosome 16 murine models of DS and suggest a causative role of DYRK1A in mental retardation and in motor anomalies of DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362710.RADtsOL4FC3SpyxB9ulzDKfGqwDIf9fFU0jbEZ1YN2ok8130_provenance.