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- NP1143490.RAhcVwh967erdAbuvQ_JBJvpy-NXkG2USwh2xX5CAivVI130_assertion type Assertion NP1143490.RAhcVwh967erdAbuvQ_JBJvpy-NXkG2USwh2xX5CAivVI130_head.
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- NP1143490.RAhcVwh967erdAbuvQ_JBJvpy-NXkG2USwh2xX5CAivVI130_assertion SIO_000772 24405844 NP1143490.RAhcVwh967erdAbuvQ_JBJvpy-NXkG2USwh2xX5CAivVI130_provenance.
- NP1143490.RAhcVwh967erdAbuvQ_JBJvpy-NXkG2USwh2xX5CAivVI130_assertion evidence source_evidence_literature NP1143490.RAhcVwh967erdAbuvQ_JBJvpy-NXkG2USwh2xX5CAivVI130_provenance.
- NP1143490.RAhcVwh967erdAbuvQ_JBJvpy-NXkG2USwh2xX5CAivVI130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1143490.RAhcVwh967erdAbuvQ_JBJvpy-NXkG2USwh2xX5CAivVI130_provenance.