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- NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_assertion type Assertion NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_head.
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- NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_assertion SIO_000772 18627422 NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.
- NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_assertion evidence source_evidence_literature NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.
- NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_assertion description "[Mutation in PAX3 causes Waardenburg syndrome, and craniofacial-deafness-hand syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682182.RATh-c9-vl1tW0opzizkD2yBTDbLvwUoj1VZrJgvVhJbU130_provenance.