Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_provenance.
- NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_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." NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_provenance.
- NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_assertion evidence source_evidence_curated NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_provenance.
- NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_assertion SIO_000772 12633764 NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_provenance.
- NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_assertion wasDerivedFrom uniprot-2016 NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_provenance.
- NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_assertion wasGeneratedBy ECO_0000218 NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP2574.RAjb0D2yJi02D4hfH7CVY1R94QLVar6EGZNnQYBAgyG80130_provenance.