Matches in Nanopublications for { ?s ?p "[The common phenotype of nuclear receptor superfamily 5, group A, member 1 (NR5A1) gene mutations in 46,XY is gonadal dysgenesis without adrenal deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The common phenotype of nuclear receptor superfamily 5, group A, member 1 (NR5A1) gene mutations in 46,XY is gonadal dysgenesis without adrenal deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1247808.RAixZMGhH-zbO7xKAvX5Zd6ChDRyhSV5zSE90SXOlpotU130_assertion description "[The common phenotype of nuclear receptor superfamily 5, group A, member 1 (NR5A1) gene mutations in 46,XY is gonadal dysgenesis without adrenal deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247808.RAixZMGhH-zbO7xKAvX5Zd6ChDRyhSV5zSE90SXOlpotU130_provenance.
- NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_assertion description "[The common phenotype of nuclear receptor superfamily 5, group A, member 1 (NR5A1) gene mutations in 46,XY is gonadal dysgenesis without adrenal deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance.