Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_assertion> ?p ?o ?g. }
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- NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_assertion type Assertion NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_head.
- 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.