assertion retraction graph subject predicate object datatype annotation 1 0 graph ONTIE:0003571 IAO:0000115 An assay measuring antibody affinity for FcRn receptor on human cells using median fluorescence intensity xsd:string 1 0 graph ONTIE:0003560 IAO:0000115 A neutralization assay measuring the IC90 of the tested antibody in ug/mL xsd:string 1 0 graph DOID:48 IAO:0000115 A reproductive system disease that affects male reproductive organs. xsd:string 1 0 graph DOID:15 IAO:0000115 A disease of anatomical entity that is located_in reproductive system organs. xsd:string 1 0 graph ONTIE:0003581 IAO:0000115 The maximum value that can be obtained. xsd:string 1 0 graph ONTIE:0003570 IAO:0000115 An assay measuring antibody affinity for FcgR3b receptor on human cells using median fluorescence intensity xsd:string 1 0 graph DOID:225 IAO:0000115 A disease characterized by a group of signs and symptoms that occur together and characterize a particular abnormality. xsd:string 1 0 graph DOID:863 IAO:0000115 A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system. xsd:string 1 0 graph ONTIE:0003580 IAO:0000115 The inflection point. xsd:string 1 0 graph DOID:0014667 IAO:0000115 A disease that involving errors in metabolic processes of building or degradation of molecules. xsd:string 1 0 graph DOID:10003 IAO:0000115 An inner ear disease that is characterized by hearing loss resulting from damage to the cochlea, auditory nerve and/or brainstem. xsd:string 1 0 graph DOID:4 IAO:0000115 A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. xsd:string 1 0 graph DOID:0040088 IAO:0000115 An autoimmune disease of eyes, ear, nose and throat that is located_in the uvea. xsd:string 1 0 graph ONTIE:0003590 IAO:0000115 An in vivo protection assay based on viral titer in lung tissue measured in PFU/ml. xsd:string 1 0 graph DOID:630 IAO:0000115 A disease that has_material_basis_in genetic variations in the human genome. xsd:string 1 0 graph DOID:2377 IAO:0000115 A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. xsd:string 1 0 graph DOID:14566 IAO:0000115 A disease that is characterized by abnormally rapid cell division. xsd:string 1 0 graph DOID:77 IAO:0000115 A disease of anatomical entity that is located_in the gastrointestinal tract. xsd:string 1 0 graph DOID:3355 IAO:0000115 A connective tissue cancer that has_material_basis_in fibrous connective tissue and characterized by the presence of immature proliferating fibroblasts or undifferentiated anaplastic spindle cells in a storiform pattern. xsd:string 1 0 graph DOID:0040095 IAO:0000115 An autoimmune disease of cardiovascular system that is characterized by deterioration of the function of the heart muscle. xsd:string