Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_assertion> ?p ?o ?g. }
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- NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_assertion type Assertion NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_head.
- NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_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." NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_provenance.
- NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_assertion evidence source_evidence_literature NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_provenance.
- NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_assertion SIO_000772 10512674 NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_provenance.
- NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_assertion wasDerivedFrom befree-20150227 NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_provenance.
- NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_assertion wasGeneratedBy ECO_0000203 NP792517.RAVc6QJJZRXvNouvgCpk9HLwsvb3wk1BYip2bBbGibzW0130_provenance.