Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_assertion> ?p ?o ?g. }
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- NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_assertion type Assertion NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_head.
- NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_assertion wasGeneratedBy ECO_0000218 NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_provenance.
- NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_assertion wasDerivedFrom uniprot-20130724 NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_provenance.
- NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_assertion SIO_000772 15562009 NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_provenance.
- NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_assertion evidence source_evidence_curated NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_provenance.
- NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_assertion description "[Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3433.RAC8V0CLdp1NQzPBq12dXJqTQYJTuCU-2GPAVhmTKy4ks130_provenance.