Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_assertion> ?p ?o ?g. }
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- NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_assertion type Assertion NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_head.
- NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_assertion wasGeneratedBy ECO_0000203 NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_provenance.
- NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_assertion wasDerivedFrom befree-2016 NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_provenance.
- NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_assertion SIO_000772 10512674 NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_provenance.
- NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_assertion evidence source_evidence_literature NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_provenance.
- NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_assertion description "[Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_provenance.