Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_assertion> ?p ?o ?g. }
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- NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_assertion type Assertion NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_head.
- NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_assertion description "[Variable phenotype in five patients with Wolcott-Rallison syndrome due to the same EIF2AK3 (c.1259delA) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_provenance.
- NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_assertion evidence source_evidence_literature NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_provenance.
- NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_assertion SIO_000772 23585173 NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_provenance.
- NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_assertion wasDerivedFrom befree-2016 NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_provenance.
- NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_assertion wasGeneratedBy ECO_0000203 NP1069158.RARPtMYHldMUuPSCihpYBBlPkzGX9C28EcNRXxhEJzu50130_provenance.