Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_provenance.
• NP18454.RATX8zp1qgxY1XNWIwDlv9GUxuizDzTLvK1etKtuN8x5s130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18454.RATX8zp1qgxY1XNWIwDlv9GUxuizDzTLvK1etKtuN8x5s130_provenance.
• NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_provenance.
• NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_provenance.
• NP18458.RAxTu_HHoQXXD1NwsNl6uOvG0WcZt6XowOPQIr28oPDuI130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18458.RAxTu_HHoQXXD1NwsNl6uOvG0WcZt6XowOPQIr28oPDuI130_provenance.
• NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_provenance.
• NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_provenance.
• NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance.
• NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance.
• assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_provenance.
• NP4756.RAENVlWeFdCPGZZS2se2kGAotJY_xP6adpSlxkbbNj-_0130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4756.RAENVlWeFdCPGZZS2se2kGAotJY_xP6adpSlxkbbNj-_0130_provenance.
• NP18456.RAG_kt57mOERpLk2UGE0t2mYyqhhQBYVcN5-mZla6JIWE130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18456.RAG_kt57mOERpLk2UGE0t2mYyqhhQBYVcN5-mZla6JIWE130_provenance.
• NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_provenance.
• NP26207.RAPYpE27agIMvUeHIeqxjXbMDHaG1jX-5h3xO-6q9La4M130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26207.RAPYpE27agIMvUeHIeqxjXbMDHaG1jX-5h3xO-6q9La4M130_provenance.
• NP26211.RAK3PCnl2Fea7FONaY9Wbp6EKebiXWFup7QZ_LsdxmI_E130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26211.RAK3PCnl2Fea7FONaY9Wbp6EKebiXWFup7QZ_LsdxmI_E130_provenance.
• NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_provenance.