Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_assertion> ?p ?o ?g. }
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- NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_assertion type Assertion NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_head.
- NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_assertion description "[Mutations in SCO2, a cytochrome c oxidase (COX) assembly gene located on chromosome 22, have recently been reported in patients with fatal infantile cardio-encephalomyopathy and severe COX deficiency in heart and skeletal muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_provenance.
- NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_assertion evidence source_evidence_literature NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_provenance.
- NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_assertion SIO_000772 10749987 NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_provenance.
- NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_assertion wasDerivedFrom befree-20140225 NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_provenance.
- NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_assertion wasGeneratedBy ECO_0000203 NP477455.RA5gNwzhGFoQh92LA4goZkQSJuB7-lH9GW8lAmVZ3e6A8130_provenance.