Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_provenance.
- NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_assertion description "[3-Methylcrotonyl-CoA carboxylase deficiency: mutation analysis in 28 probands, 9 symptomatic and 19 detected by newborn screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_provenance.
- NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_assertion evidence source_evidence_curated NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_provenance.
- NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_assertion SIO_000772 16010683 NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_provenance.
- NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_assertion wasDerivedFrom uniprot-20150221 NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_provenance.
- NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_assertion wasGeneratedBy ECO_0000218 NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4769.RATw1C7PB1dYH_lLCgvNEIfYxlMnZEsVmLtBXlvhXRHTY130_provenance.