Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_provenance.
- NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_assertion description "[As in other metabolic disorders, the distinction between 'normal' and 'disease' in MCAD deficiency is blurring into a spectrum of enzyme deficiency states caused by different mutations in the ACADM gene potentially influenced by factors affecting intracellular protein processing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_provenance.
- NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_assertion evidence source_evidence_curated NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_provenance.
- NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_assertion SIO_000772 11409868 NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_provenance.
- NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_assertion wasDerivedFrom uniprot-20150221 NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_provenance.
- NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_assertion wasGeneratedBy ECO_0000218 NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1504.RA8ro9E42BQOMiv4IjKL8c3--MGitQcouXQ8gp7MzLVws130_provenance.