Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_assertion type Assertion NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_head.
- NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_assertion description "[It has been known for some time that loss of function mutations in KCNJ11, which encodes for Kir6.2, and ABCC8, which encodes for SUR1, can cause oversecretion of insulin and result in hyperinsulinism of infancy, while activating mutations in KCNJ11 and ABCC8 have recently been described that result in the opposite phenotype of diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_provenance.
- NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_assertion evidence source_evidence_literature NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_provenance.
- NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_assertion SIO_000772 18767144 NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_provenance.
- NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_assertion wasDerivedFrom befree-20140225 NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_provenance.
- NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_assertion wasGeneratedBy ECO_0000203 NP218400.RA29qmAfU0U89omOqs0ZtoD87Fw6MEvZ7Z3F6Hd6-z2fI130_provenance.