Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_assertion> ?p ?o ?g. }
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- NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_assertion type Assertion NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_head.
- NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_assertion wasGeneratedBy ECO_0000203 NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_provenance.
- NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_assertion wasDerivedFrom befree-2016 NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_provenance.
- NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_assertion SIO_000772 15579781 NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_provenance.
- NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_assertion evidence source_evidence_literature NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_provenance.
- NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_assertion description "[Hyperinsulinism of infancy is a genetically heterogeneous disease characterized by dysregulation of insulin secretion resulting in severe hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471296.RAuev3PpPZeK-_ZMbfAePPB-jVuIzxwCbMQJO1JR8Rtoo130_provenance.