Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_assertion> ?p ?o ?g. }
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- NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_assertion type Assertion NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_head.
- NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_assertion description "[Deficiency of ornithine-delta-aminotransferase (OAT) in humans causes hyperornithinaemia and gyrate atrophy (GA), a blinding chorioretinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_provenance.
- NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_assertion evidence source_evidence_literature NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_provenance.
- NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_assertion SIO_000772 7550347 NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_provenance.
- NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_assertion wasDerivedFrom befree-2016 NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_provenance.
- NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_assertion wasGeneratedBy ECO_0000203 NP1312183.RAE71-iduD0VeD49qXoMioVFNAmoiOPmXOtKpoEYjFQJc130_provenance.