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- NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_assertion type Assertion NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_head.
- NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_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." NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_provenance.
- NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_assertion evidence source_evidence_literature NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_provenance.
- NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_assertion SIO_000772 2549843 NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_provenance.
- NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_assertion wasDerivedFrom befree-20140225 NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_provenance.
- NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_assertion wasGeneratedBy ECO_0000203 NP600632.RA2Fv12PwwH6TmYNNk4j6i2Oyco0HNeNmtSHJKz0kq7YQ130_provenance.