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- NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_assertion type Assertion NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_head.
- NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_provenance.
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- NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_assertion SIO_000772 18264947 NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_provenance.
- NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_assertion wasDerivedFrom gad-20150221 NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_provenance.
- NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_assertion wasGeneratedBy ECO_0000203 NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_provenance.