Matches in Nanopublications for { ?s ?p "[The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of a member of the GATA-binding family of transcription factors, GATA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of a member of the GATA-binding family of transcription factors, GATA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of a member of the GATA-binding family of transcription factors, GATA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP480541.RAbdnQKH2vEhoikYFy3xIwpxsu2Csgj-3lb0SJQFljibg130_assertion description "[The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of a member of the GATA-binding family of transcription factors, GATA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480541.RAbdnQKH2vEhoikYFy3xIwpxsu2Csgj-3lb0SJQFljibg130_provenance.
- NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_assertion description "[The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of a member of the GATA-binding family of transcription factors, GATA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_provenance.
- NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_assertion description "[The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of a member of the GATA-binding family of transcription factors, GATA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance.
- NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_assertion description "[The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of a member of the GATA-binding family of transcription factors, GATA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance.