Raman Spectroscopy is an excellent method to characterize carbon nanomaterials. Its fairly complex so I am going to try to explain this in a very simple language. The ratio of intensity of D/G bands is a measure of the defects present on graphene structure. The G band is a result of in-plane vibrations of SP2 bonded carbon atoms whereas the D band is due to out of plane vibrations attributed to the presence of structural defects. Now, when you compare the spectra of graphene and graphene oxide, GO will have a higher D band. This is due to the disruption of SP2 bonds of the carbon as GO has oxidative functional groups.
So, if the D band is higher, it means that the SP2 bonds are broken which in turn means that there are more SP3 bonds. However, D band can be present due to various other reasons. So if your D/G ratio is higher than pristine graphene, it means that there are defects. It does not mean that you have more SP3 than SP2 in the same sample. It shows that you have more SP3 in GO compared to pristine graphene.
You can also try high resolution XPS which can give you elemental quantification and see what functional groups are present.
The limitation of Raman and XPS both is that these are point - surface - techniques. This means that you are only measuring a very small region of the entire sample, precisely a point that is on the surface. However, this is an accepted limitation of these techniques and therefore I would be very careful before drawing any firm conclusions. Its better to do two types of chemical characterization than just doing one. That way you can be more sure of your data.
In my recent paper I have compared Raman spectra of single layer graphene and single layer graphene oxide with different oxygen content. It will help you.