Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_provenance.
- NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_assertion description "[Multiple carboxylase deficiency (MCD, MIM:253270) is a common organic aciduria and caused by deficiency of either biotinidase or holocarboxylase synthetase (HLCS; EC 6.3.4.10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_provenance.
- NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_assertion evidence source_evidence_literature NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_provenance.
- NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_assertion SIO_000772 12633764 NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_provenance.
- NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_assertion wasDerivedFrom befree-2016 NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_provenance.
- NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_assertion wasGeneratedBy ECO_0000203 NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_provenance.
- befree-2016 importedOn "2016-02-19" NP386889.RATjDKi4-E9xZtPi73EPiyxjDFaVzCyRRYKzc_jgb9sog130_provenance.