Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_provenance.
- NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_assertion description "[Isolated 3-methylcrotonyl-CoA carboxylase (MCC) deficiency is an autosomal recessive disorder that appears to be the most frequent organic aciduria detected in tandem mass spectrometry (TMS)-based neonatal screening programs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_provenance.
- NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_assertion evidence source_evidence_literature NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_provenance.
- NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_assertion SIO_000772 16010683 NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_provenance.
- NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_assertion wasDerivedFrom befree-20140225 NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_provenance.
- NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_assertion wasGeneratedBy ECO_0000203 NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478682.RAQjbgLYRGDGV99gbTju09GrjmnZvc2qE7YIKNGWTD-ZA130_provenance.