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- source_evidence_literature type ECO_0000212 NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP964011.RAG36f10wgByw2IB_oHQv8f4ycG9nnk6pLhuFR7SA4eRM130_provenance.