Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_assertion> ?p ?o ?g. }
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- NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_assertion type Assertion NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_head.
- NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_assertion wasGeneratedBy ECO_0000203 NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_provenance.
- NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_assertion wasDerivedFrom befree-2016 NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_provenance.
- NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_assertion SIO_000772 21872273 NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_provenance.
- NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_assertion evidence source_evidence_literature NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_provenance.
- NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_assertion description "[In this study, we screened a French cohort of patients with Sjögren-Larsson syndrome (SLS) for mutations in the ALDH3A2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919607.RAk91e9Ffs302Mdpi1g3M2EmYKDi8sQy7DdYZ2XgUn0FE130_provenance.