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- NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_assertion type Assertion NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_head.
- NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_assertion wasGeneratedBy ECO_0000203 NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_provenance.
- NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_assertion wasDerivedFrom befree-2016 NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_provenance.
- NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_assertion SIO_000772 23335808 NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_provenance.
- NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_assertion evidence source_evidence_literature NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_provenance.
- NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_provenance.