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- NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_assertion type Assertion NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_head.
- NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_provenance.
- NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_assertion evidence source_evidence_literature NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_provenance.
- NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_assertion SIO_000772 18575922 NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_provenance.
- NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_assertion wasDerivedFrom befree-2016 NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_provenance.
- NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_assertion wasGeneratedBy ECO_0000203 NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_provenance.