Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_provenance.
- NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_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." NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_provenance.
- NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_assertion evidence source_evidence_literature NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_provenance.
- NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_assertion SIO_000772 11161836 NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_provenance.
- NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_assertion wasDerivedFrom befree-20140225 NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_provenance.
- NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_assertion wasGeneratedBy ECO_0000203 NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP751491.RAwynNzFQLHQEh9DTH0PFywwY7sZC_Np7cNYmp59Zquqs130_provenance.