Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_provenance.
- NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_assertion wasGeneratedBy ECO_0000218 NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_provenance.
- NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_assertion wasDerivedFrom uniprot-2016 NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_provenance.
- NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_assertion SIO_000772 10647889 NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_provenance.
- NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_assertion evidence source_evidence_curated NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_provenance.
- NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_assertion description "[Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600.RADqCRnXPhvDDZ7iYkr-NOwBInKyBen-PfaxZPdnQ7Z0g130_provenance.