Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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." provenance.
- 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." provenance.
- 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." provenance.
- 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.
- NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_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." NP650613.RAUcZx3wmjjv3IGSZEj8K18BK8cNfhRbInmZjRxJhkZOo130_provenance.
- NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_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." NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance.
- NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_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." NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_provenance.