Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_assertion> ?p ?o ?g. }
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- NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_assertion type Assertion NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_head.
- NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_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." NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_provenance.
- NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_assertion evidence source_evidence_literature NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_provenance.
- NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_assertion SIO_000772 2549843 NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_provenance.
- NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_assertion wasDerivedFrom befree-20140225 NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_provenance.
- NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_assertion wasGeneratedBy ECO_0000203 NP630100.RAHPwdHQmh8ETB3D8nwMKLQrh3zIHWpBbho8cveC_lxaQ130_provenance.