Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_provenance.
- NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_assertion description "[Identification of four novel mutations in patients with carnitine palmitoyltransferase II (CPT II) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_provenance.
- NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_assertion evidence source_evidence_curated NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_provenance.
- NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_assertion SIO_000772 9758712 NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_provenance.
- NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_assertion wasDerivedFrom uniprot-2016 NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_provenance.
- NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_assertion wasGeneratedBy ECO_0000218 NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9893.RAP6MTWsS0S5X-JCBxFg9WH9eOqMMq4cFWUeeNGvt96pY130_provenance.