Matches in Nanopublications for { ?s ?p "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP936129.RAuqMWG1EdFs2IZHB5ZC3aDED1pk1hkdM83YjiwW5AZ1s130_assertion description "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936129.RAuqMWG1EdFs2IZHB5ZC3aDED1pk1hkdM83YjiwW5AZ1s130_provenance.
- NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_assertion description "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936145.RAiFICHxcAY5ToY9hMp9klX9hgIcrfI1mwkW-obpxTLIg130_provenance.
- NP1081110.RAUdChVOStT5g2I8aGDXxQU0lGdWeK0PrHTuvKB521z18130_assertion description "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081110.RAUdChVOStT5g2I8aGDXxQU0lGdWeK0PrHTuvKB521z18130_provenance.
- NP936139.RADhylJV9-nCI1DCS5R2B3qng63bgBWqGtXAldZsAnMic130_assertion description "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936139.RADhylJV9-nCI1DCS5R2B3qng63bgBWqGtXAldZsAnMic130_provenance.
- NP1081106.RAoW909dp6g-aqOFG0Dt1k43Vmmfcv_mnpVrMZXjFT-OU130_assertion description "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081106.RAoW909dp6g-aqOFG0Dt1k43Vmmfcv_mnpVrMZXjFT-OU130_provenance.
- NP1081109.RA-xf-VRE3R__TYcfG2zh7sucUnBb5RWhpnAJL1x828nY130_assertion description "[Recessive mutations in FKBP10 at 17q21.2, encoding FKBP65, cause both osteogenesis imperfecta (OI) and Bruck syndrome (OI plus congenital contractures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081109.RA-xf-VRE3R__TYcfG2zh7sucUnBb5RWhpnAJL1x828nY130_provenance.