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- NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_assertion type Assertion NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_head.
- NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_provenance.
- NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_assertion evidence source_evidence_literature NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_provenance.
- NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_assertion SIO_000772 23911094 NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_provenance.
- NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_assertion wasDerivedFrom befree-2016 NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_provenance.
- NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_assertion wasGeneratedBy ECO_0000203 NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_provenance.