Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_assertion> ?p ?o ?g. }
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- NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_assertion type Assertion NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_head.
- NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_assertion description "[Heterozygous inactivating mutations in the glucokinase gene (GCK) cause a mild form of diabetes (maturity-onset diabetes of the young [MODY]2), and activating mutations have been associated with a mild form of familial hyperinsulinemic hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.
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- NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_assertion SIO_000772 15277402 NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.
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