Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_assertion type Assertion NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_head.
- NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_assertion description "[Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare, autosomal recessive disease of unregulated insulin secretion, defined by elevations in serum insulin despite severe hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_provenance.
- NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_assertion evidence source_evidence_literature NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_provenance.
- NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_assertion SIO_000772 7847376 NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_provenance.
- NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_assertion wasDerivedFrom befree-2016 NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_provenance.
- NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_assertion wasGeneratedBy ECO_0000203 NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_provenance.