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- NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_assertion type Assertion NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_head.
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- NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_assertion wasDerivedFrom befree-20150227 NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_assertion SIO_000772 23539225 NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_assertion evidence source_evidence_literature NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_assertion description "[Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.