Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion> ?p ?o ?g. }
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- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion type Assertion NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_head.
- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion wasGeneratedBy ECO_0000218 NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion wasDerivedFrom uniprot-2016 NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion SIO_000772 15562009 NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion evidence source_evidence_curated NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_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." NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.