Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_provenance.
- NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_assertion description "[The clinical phenotype and outcome of mitochondrial acetoacetyl-CoA thiolase deficiency (beta-ketothiolase or T2 deficiency) in 26 enzymatically proved and mutation-defined patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_provenance.
- NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_assertion evidence source_evidence_literature NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_provenance.
- NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_assertion SIO_000772 11161836 NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_provenance.
- NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_assertion wasDerivedFrom befree-2016 NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_provenance.
- NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_assertion wasGeneratedBy ECO_0000203 NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_provenance.
- befree-2016 importedOn "2016-02-19" NP305938.RA_C_TtmbgLmrVu0msRNpG67dEOQkArKPOa3oSX52Fgd0130_provenance.