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HarmPot: An Annotation Framework for Evaluating Offline Harm Potential of Social Media Text

arXiv.org Artificial Intelligence

In this paper, we discuss the development of an annotation schema to build datasets for evaluating the offline harm potential of social media texts. We define "harm potential" as the potential for an online public post to cause real-world physical harm (i.e., violence). Understanding that real-world violence is often spurred by a web of triggers, often combining several online tactics and pre-existing intersectional fissures in the social milieu, to result in targeted physical violence, we do not focus on any single divisive aspect (i.e., caste, gender, religion, or other identities of the victim and perpetrators) nor do we focus on just hate speech or mis/dis-information. Rather, our understanding of the intersectional causes of such triggers focuses our attempt at measuring the harm potential of online content, irrespective of whether it is hateful or not. In this paper, we discuss the development of a framework/annotation schema that allows annotating the data with different aspects of the text including its socio-political grounding and intent of the speaker (as expressed through mood and modality) that together contribute to it being a trigger for offline harm. We also give a comparative analysis and mapping of our framework with some of the existing frameworks.


Google DeepMind AI tool assesses DNA mutations for harm potential

The Guardian

Scientists at Google DeepMind have built an artificial intelligence program that can predict whether millions of genetic mutations are either harmless or likely to cause disease, in an effort to speed up research and the diagnosis of rare disorders. The program makes predictions about so-called missense mutations, where a single letter is misspelt in the DNA code. Such mutations are often harmless but they can disrupt how proteins work and cause diseases from cystic fibrosis and sickle-cell anaemia to cancer and problems with brain development. The researchers used AlphaMissense to assess all 71m single-letter mutations that could affect human proteins. When they set the program's precision to 90%, it predicted that 57% of missense mutations were probably harmless and 32% were probably harmful. It was uncertain about the impact of the rest.