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- NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_assertion type Assertion NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_head.
- NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_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." NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_provenance.
- NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_assertion evidence source_evidence_literature NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_provenance.
- NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_assertion SIO_000772 18264947 NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_provenance.
- NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_assertion wasDerivedFrom gad-20130706 NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_provenance.
- NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_assertion wasGeneratedBy ECO_0000203 NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_provenance.