Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_assertion> ?p ?o ?g. }
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- NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_assertion type Assertion NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_head.
- NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_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." NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_provenance.
- NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_assertion evidence source_evidence_literature NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_provenance.
- NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_assertion SIO_000772 7550347 NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_provenance.
- NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_assertion wasDerivedFrom befree-20150227 NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_provenance.
- NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_assertion wasGeneratedBy ECO_0000203 NP601386.RAv6A1drtiX9GmA8vqrbqqSknGQlCNpuyE4zQeBBgOpFk130_provenance.