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- NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_assertion type Assertion NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_head.
- NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_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." NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_provenance.
- NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_assertion evidence source_evidence_literature NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_provenance.
- NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_assertion SIO_000772 18264947 NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_provenance.
- NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_assertion wasDerivedFrom gad-20150221 NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_provenance.
- NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_assertion wasGeneratedBy ECO_0000203 NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_provenance.