Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_provenance.
- NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_assertion description "[Mitochondrial acetoacetyl-CoA thiolase (T2 enzyme) deficiency (MIM 203750) is an autosomal recessive disorder of isoleucine and ketone-body metabolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_provenance.
- NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_assertion evidence source_evidence_literature NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_provenance.
- NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_assertion SIO_000772 11161836 NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_provenance.
- NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_assertion wasDerivedFrom befree-20140225 NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_provenance.
- NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_assertion wasGeneratedBy ECO_0000203 NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP847607.RAh9iIRXHS7GfB4Q89NnwBYknUHIS6WXdXiQd39LVsO1w130_provenance.