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- NP55567.RAjxJXiNs2CaHIDvbEIUUT8_KAQb9on4-NrlsklbgX7Fs130_assertion type Assertion NP55567.RAjxJXiNs2CaHIDvbEIUUT8_KAQb9on4-NrlsklbgX7Fs130_head.
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- NP55567.RAjxJXiNs2CaHIDvbEIUUT8_KAQb9on4-NrlsklbgX7Fs130_assertion wasDerivedFrom gad-20130706 NP55567.RAjxJXiNs2CaHIDvbEIUUT8_KAQb9on4-NrlsklbgX7Fs130_provenance.
- NP55567.RAjxJXiNs2CaHIDvbEIUUT8_KAQb9on4-NrlsklbgX7Fs130_assertion SIO_000772 14517947 NP55567.RAjxJXiNs2CaHIDvbEIUUT8_KAQb9on4-NrlsklbgX7Fs130_provenance.
- NP55567.RAjxJXiNs2CaHIDvbEIUUT8_KAQb9on4-NrlsklbgX7Fs130_assertion evidence source_evidence_literature NP55567.RAjxJXiNs2CaHIDvbEIUUT8_KAQb9on4-NrlsklbgX7Fs130_provenance.
- NP55567.RAjxJXiNs2CaHIDvbEIUUT8_KAQb9on4-NrlsklbgX7Fs130_assertion description "[These results provide substantial evidence that genetic variation within or extremely close to IDE impacts both disease risk and traits related to the severity of AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55567.RAjxJXiNs2CaHIDvbEIUUT8_KAQb9on4-NrlsklbgX7Fs130_provenance.