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- NP794367.RAR1oljVkTI29jw11xyfzGQD5O1dBuDw6JahQd7g-WdY4130_assertion type Assertion NP794367.RAR1oljVkTI29jw11xyfzGQD5O1dBuDw6JahQd7g-WdY4130_head.
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- NP794367.RAR1oljVkTI29jw11xyfzGQD5O1dBuDw6JahQd7g-WdY4130_assertion SIO_000772 22878500 NP794367.RAR1oljVkTI29jw11xyfzGQD5O1dBuDw6JahQd7g-WdY4130_provenance.
- NP794367.RAR1oljVkTI29jw11xyfzGQD5O1dBuDw6JahQd7g-WdY4130_assertion evidence source_evidence_literature NP794367.RAR1oljVkTI29jw11xyfzGQD5O1dBuDw6JahQd7g-WdY4130_provenance.
- NP794367.RAR1oljVkTI29jw11xyfzGQD5O1dBuDw6JahQd7g-WdY4130_assertion description "[A BAP1 catalytic mutation found in a MDS patient implies that BAP1 loss of function has similar consequences in mice and humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794367.RAR1oljVkTI29jw11xyfzGQD5O1dBuDw6JahQd7g-WdY4130_provenance.