Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_assertion> ?p ?o ?g. }
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- NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_assertion type Assertion NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_head.
- NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_assertion description "[These findings demonstrate that the range of the clinical phenotype caused by GCK mutations varies from complete insulin deficiency to extreme hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_provenance.
- NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_assertion evidence source_evidence_literature NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_provenance.
- NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_assertion SIO_000772 15277402 NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_provenance.
- NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_assertion wasDerivedFrom befree-20140225 NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_provenance.
- NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_assertion wasGeneratedBy ECO_0000203 NP747016.RAfpunTUhWK5WhtD7Oimyr9xqv_g-vQnOi1HH0-o0vwxw130_provenance.