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- NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_assertion type Assertion NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_head.
- NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_assertion description "[Mutations in human AHI1 underlie the autosomal recessive Joubert Syndrome with brain malformation and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
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- NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_assertion SIO_000772 16773125 NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
- NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_assertion wasDerivedFrom befree-20150227 NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.
- NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_assertion wasGeneratedBy ECO_0000203 NP914397.RAIZr_f52Offf0He7DGegJrbw95cWMED9f6ednyvnZJwM130_provenance.