Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance.
- NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance.
- NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_assertion evidence source_evidence_curated NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance.
- NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_assertion SIO_000772 10749987 NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance.
- NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_assertion wasDerivedFrom uniprot-20130724 NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance.
- NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_assertion wasGeneratedBy ECO_0000218 NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance.