Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_assertion> ?p ?o ?g. }
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- NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_assertion type Assertion NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_head.
- NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_assertion wasGeneratedBy ECO_0000203 NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_provenance.
- NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_assertion wasDerivedFrom lhgdn-20090331 NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_provenance.
- NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_assertion SIO_000772 15235026 NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_provenance.
- NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_assertion evidence source_evidence_literature NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_provenance.
- NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_assertion description "[A patient with typical clinical and neuroradiological features of Leigh syndrome and cytochrome oxidase deficiency was found to have a mutation in the COX15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205777.RAPb0I12grRESFUAaDkApiUo6XmpQh5nqJm9ALSHOSZ9s130_provenance.