Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion> ?p ?o ?g. }
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- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion type Assertion NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_head.
- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion description "[A point mutation or a small deletion of mitochondrial DNA, probably affecting the COX-II gene, may be responsible for the COX deficiency in this case of MERRF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion evidence source_evidence_literature NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion SIO_000772 2549843 NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion wasDerivedFrom befree-20140225 NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion wasGeneratedBy ECO_0000203 NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.