Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion type Assertion NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_head.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion description "[Infantile cerebellar-retinal degeneration associated with a mutation in mitochondrial aconitase, ACO2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion evidence source_evidence_literature NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion SIO_000772 22405087 NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion wasDerivedFrom befree-2016 NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion wasGeneratedBy ECO_0000203 NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.