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- NP208095.RAAkjxw6iCg3vL_G0wlcDlVzRk9oeR3VHNAxLQf3YDbqo130_assertion type Assertion NP208095.RAAkjxw6iCg3vL_G0wlcDlVzRk9oeR3VHNAxLQf3YDbqo130_head.
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- NP208095.RAAkjxw6iCg3vL_G0wlcDlVzRk9oeR3VHNAxLQf3YDbqo130_assertion wasDerivedFrom lhgdn-20090331 NP208095.RAAkjxw6iCg3vL_G0wlcDlVzRk9oeR3VHNAxLQf3YDbqo130_provenance.
- NP208095.RAAkjxw6iCg3vL_G0wlcDlVzRk9oeR3VHNAxLQf3YDbqo130_assertion SIO_000772 15580558 NP208095.RAAkjxw6iCg3vL_G0wlcDlVzRk9oeR3VHNAxLQf3YDbqo130_provenance.
- NP208095.RAAkjxw6iCg3vL_G0wlcDlVzRk9oeR3VHNAxLQf3YDbqo130_assertion evidence source_evidence_literature NP208095.RAAkjxw6iCg3vL_G0wlcDlVzRk9oeR3VHNAxLQf3YDbqo130_provenance.
- NP208095.RAAkjxw6iCg3vL_G0wlcDlVzRk9oeR3VHNAxLQf3YDbqo130_assertion description "[KCNJ11 mutations are a common cause of permanent neonatal diabetes mellitus either in isolation or associated with developmental delay ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208095.RAAkjxw6iCg3vL_G0wlcDlVzRk9oeR3VHNAxLQf3YDbqo130_provenance.