Matches in Nanopublications for { ?s ?p "[Camurati-Engelmann disease (CED, MIM 131300) is an autosomal dominant, progressive diaphyseal dysplasia characterized by hyperosteosis and sclerosis of the diaphyses of long bones.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Camurati-Engelmann disease (CED, MIM 131300) is an autosomal dominant, progressive diaphyseal dysplasia characterized by hyperosteosis and sclerosis of the diaphyses of long bones.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_assertion description "[Camurati-Engelmann disease (CED, MIM 131300) is an autosomal dominant, progressive diaphyseal dysplasia characterized by hyperosteosis and sclerosis of the diaphyses of long bones.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_provenance.
- NP294144.RApOCgI7CNkhEbhyLbyodwQ6G6GCdP_vApw0C21v4gY14130_assertion description "[Camurati-Engelmann disease (CED, MIM 131300) is an autosomal dominant, progressive diaphyseal dysplasia characterized by hyperosteosis and sclerosis of the diaphyses of long bones.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294144.RApOCgI7CNkhEbhyLbyodwQ6G6GCdP_vApw0C21v4gY14130_provenance.