Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_provenance.
- NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_assertion description "[Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_provenance.
- NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_assertion evidence source_evidence_literature NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_provenance.
- NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_assertion SIO_000772 24341803 NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_provenance.
- NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_assertion wasDerivedFrom befree-20150227 NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_provenance.
- NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_assertion wasGeneratedBy ECO_0000203 NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP907341.RAje1NI7HApCJgXijNrYb0FE36CoKBxPmBTorcR6dXEgA130_provenance.