Matches in Nanopublications for { ?s ?p "[Context: Steroid 21-hydroxylase deficiency is the most common enzymatic defect causing congenital adrenal hyperplasia with genotype/phenotype relationships for common mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Context: Steroid 21-hydroxylase deficiency is the most common enzymatic defect causing congenital adrenal hyperplasia with genotype/phenotype relationships for common mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_assertion description "[Context: Steroid 21-hydroxylase deficiency is the most common enzymatic defect causing congenital adrenal hyperplasia with genotype/phenotype relationships for common mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance.
- NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_assertion description "[Context: Steroid 21-hydroxylase deficiency is the most common enzymatic defect causing congenital adrenal hyperplasia with genotype/phenotype relationships for common mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance.