Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_provenance.
- befree-2016 importedOn "2016-02-19" NP264823.RADevIwVojdh8tMZjwSNMZYIQv_N7e7jcF4UX1cONJbtA130_provenance.
- 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.