Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_assertion type Assertion NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_head.
- NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_assertion description "[Herein, we report the clinical phenotypes and disease-causative mutations in the ALDH7A1 gene in three Korean patients with PDE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_provenance.
- NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_assertion evidence source_evidence_literature NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_provenance.
- NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_assertion SIO_000772 22371912 NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_provenance.
- NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_assertion wasDerivedFrom befree-2016 NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_provenance.
- NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_assertion wasGeneratedBy ECO_0000203 NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_provenance.