Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_assertion> ?p ?o ?g. }
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- NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_assertion type Assertion NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_head.
- NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_assertion description "[Dyschromatosis symmetrica hereditaria (DSH) is an autosomal dominant pigmentary genodermatosis characterized by hyperpigmented and hypopigmented macules of on the extremities and caused by the mutations in the ADAR gene(also called DSRAD) encoding for RNA-specific adenosine deaminase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_provenance.
- NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_assertion evidence source_evidence_literature NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_provenance.
- NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_assertion SIO_000772 15146470 NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_provenance.
- NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_assertion wasDerivedFrom befree-20140225 NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_provenance.
- NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_assertion wasGeneratedBy ECO_0000203 NP930668.RAe8Hwevc0V69TIoR9Y2jPjFOjbsAIq0oAyu0sSnepQog130_provenance.