Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_assertion> ?p ?o ?g. }
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- NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_assertion type Assertion NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_head.
- NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_assertion description "[LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_provenance.
- NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_assertion evidence source_evidence_literature NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_provenance.
- NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_assertion SIO_000772 21266382 NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_provenance.
- NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_assertion wasDerivedFrom befree-2016 NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_provenance.
- NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_assertion wasGeneratedBy ECO_0000203 NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_provenance.