Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_assertion type Assertion NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_head.
- NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_assertion description "[Leigh syndrome associated with mitochondrial complex I deficiency due to novel mutations In NDUFV1 and NDUFS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_provenance.
- NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_assertion evidence source_evidence_literature NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_provenance.
- NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_assertion SIO_000772 23266820 NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_provenance.
- NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_assertion wasDerivedFrom befree-2016 NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_provenance.
- NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_assertion wasGeneratedBy ECO_0000203 NP1038643.RAr542UqO-W_kS5MnmS91uehOU5eDZbCLGh6NwTF7z2F0130_provenance.