Matches in Nanopublications for { ?s ?p "[Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP406001.RAvdobMjEMm5u9pCSjHXCAQLFljhDshYiaQN3whtgLXsk130_assertion description "[Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406001.RAvdobMjEMm5u9pCSjHXCAQLFljhDshYiaQN3whtgLXsk130_provenance.
- assertion description "[Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP734253.RAav_dEs5q7hBVhoDp4K37Ku2zPovXKHYzliehz_yQ9j0130_assertion description "[Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734253.RAav_dEs5q7hBVhoDp4K37Ku2zPovXKHYzliehz_yQ9j0130_provenance.
- NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_assertion description "[Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance.
- NP734258.RAp0nw7rAVYtLPNv7WyzdevH_wq9WfpdJsCP-NcuEw3Ic130_assertion description "[Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734258.RAp0nw7rAVYtLPNv7WyzdevH_wq9WfpdJsCP-NcuEw3Ic130_provenance.
- NP447378.RA1pFBURJDmlsLbQa6CHcf_xF0VR6mQj9r7Z2tSKyXNdg130_assertion description "[Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447378.RA1pFBURJDmlsLbQa6CHcf_xF0VR6mQj9r7Z2tSKyXNdg130_provenance.
- NP734252.RA0lzYvXCc8vkgarrsvmeb5mBpDRfT4DjR09UJo-Qu2Lk130_assertion description "[Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734252.RA0lzYvXCc8vkgarrsvmeb5mBpDRfT4DjR09UJo-Qu2Lk130_provenance.
- NP854758.RA3bX0zdry9oRJ2ODY4yglIWZmtPhKpFFLwa-s0ETeIek130_assertion description "[Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854758.RA3bX0zdry9oRJ2ODY4yglIWZmtPhKpFFLwa-s0ETeIek130_provenance.