325 research outputs found

    Circuit Complexity Meets Ontology-Based Data Access

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    Ontology-based data access is an approach to organizing access to a database augmented with a logical theory. In this approach query answering proceeds through a reformulation of a given query into a new one which can be answered without any use of theory. Thus the problem reduces to the standard database setting. However, the size of the query may increase substantially during the reformulation. In this survey we review a recently developed framework on proving lower and upper bounds on the size of this reformulation by employing methods and results from Boolean circuit complexity.Comment: To appear in proceedings of CSR 2015, LNCS 9139, Springe

    Towards Efficient Reasoning under Guarded-based Disjunctive Existential Rules

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    International audienceThe complete picture of the complexity of answering (unions of) conjunctive queries under the main guarded-based classes of disjunc- tive existential rules has been recently settled. It has been shown that the problem is very hard, namely 2ExpTime-complete, even for fixed sets of rules expressed in lightweight formalisms. This gives rise to the question whether its complexity can be reduced by restricting the query language. Several subclasses of conjunctive queries have been proposed with the aim of reducing the complexity of classical database problems such as query evaluation and query containment. Three of the most prominent subclasses of this kind are queries of bounded hypertree-width, queries of bounded treewidth and acyclic queries. The central objective of the present paper is to understand whether the above query languages have a positive impact on the complexity of query answering under the main guarded-based classes of disjunctive existential rules. We show that (unions of) conjunctive queries of bounded hypertree- width and of bounded treewidth do not reduce the complexity of our problem, even if we focus on predicates of bounded arity, or on fixed sets of disjunctive existential rules. Regarding acyclic queries, although our problem remains 2ExpTime-complete in general, in some relevant set- tings the complexity reduces to ExpTime-complete; in fact, this requires to bound the arity of the predicates, and for some expressive guarded- based formalisms, to fix the set of rules

    Devolatilization of organo-sulfur compounds in coal gasification

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    Coal gasification is a thermo-chemical process aiming at the production of high heating value syngas. The coal charges present, typically, a low quantity of sulfur compounds for prevent the formation of a large amount of sulfuric acid (H2S), that is a pollutant and a poison for catalysts, in syngas stream. However, in the world there are a lot of coals that cannot be used for gasification because of their high sulfur content (e.g. Sulcis Italian coal or Inner Mongolia Chinese coal). The interest on these types of coal is increasing due to a novel technology that allows to convert H2S and CO2into syngas (AG2S\u2122). The aim of this work is to propose a predictive kinetic model of the release of sulfur compounds (e.g H2S) from coal. This kinetic scheme is implement into GASDS, a package that includes a gasifier mathematical model, which accurately describes the inter-phase mass and heat transfer. The first complexity relies in the characterization of the coal, in particular the relative amount of the different forms of sulfur components (e.g. inorganic such as pyritic and sulfates, and organic sulfur such as aliphatic, aromatic and thiophenic) and their pyrolysis and devolatilization process. The kinetic model, with the related rate parameters, is validated through comparison with experimental data from the literature and obtained during several experimental campaigns at the Sotacarbo S.p.A. pilot platform. Finally, different operating conditions of gasification are analyzed in order to obtain the best yield in the downstream process, with special reference to the novel Acid Gas to Syngas (AG2STM) process

    Multiplex ligation-dependent probe amplification detection of an unknown large deletion of the CREB-binding protein gene in a patient with Rubinstein-Taybi syndrome

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    Rubinstein-Taybi syndrome is a rare autosomal dominant congenital disorder characterized by postnatal growth retardation, psychomotor developmental delay, skeletal anomalies, peculiar facial morphology, and tumorigenesis. Mutations in the gene encoding the cAMP response element-binding protein (CREB, also known as CREBBP or CBP) on chromosome 16p13.3 have been identified. In addition, some patients with low intelligence quotients and autistic features bear large deletions. Based on these observations, we used multiplex ligation-dependent probe amplification to search for large deletions affecting the CREBBP gene in a Rubinstein-Taybi syndrome patient. We identified a novel heterozygote deletion removing five exons (exons 17-21), encoding the histone acetyltransferase domain. We propose the use of multiplex ligation-dependent probe amplification as a fast, accurate and cheap test for detecting large deletions in the CREBBP gene in the sub-group of Rubinstein-Taybi syndrome patients with low intelligence quotients and autistic features

    Performance evaluation of SiPMʼs for low threshold gamma detection

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    In the context of the on-line monitoring of short and medium term for radioactive waste repository, a new system has been planned. Such system makes use a new kind of detector, named Silicon Photomultiplier, coupled to scintillating fibres to be positioned around each waste drum in shape of fine grid. The purpose of this design is evaluate the variations of the radioactivity distribution by counting the gamma radiation

    STYPES: nonrecursive datalog rewriter for linear TGDs and conjunctive queries

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    We present STYPES, a system that rewrites ontology-mediated queries with linear tuple-generating dependencies and conjunctive queries to equivalent nonrecursive datalog (NDL) queries. The main feature of STYPES is that it produces polynomial-size rewritings whenever the treewidth of the input conjunctive queries and the size of the chases for the ontology atoms as well as their arity are bounded; moreover, the rewritings can be constructed and executed in LOGCFL, indicating high parallelisability in theory. We show experimentally that Apache Flink on a cluster of machines with 20 virtual CPUs is indeed able to parallelise execution of a series of NDL-rewritings constructed by STYPES, with the time decreasing proportionally to the number of CPUs available

    Signaling through Ras is essential for ret oncogene-induced cell differentiation in PC12 cells.

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    Specific germline mutations of the receptor tyrosine kinase, Ret, predispose to multiple endocrine neoplasia types 2A and 2B and familial medullary thyroid carcinoma. The mechanisms by which different Ret isoforms (Ret-2A and Ret-2B) cause distinct neoplastic diseases remain largely unknown. On the other hand, forced expression of these mutated versions of Ret induces the rat pheochromocytoma cell line, PC12, to differentiate. Here we used an inducible vector encoding a dominant-negative Ras (Ras p21(N17)) to investigate the contributions of the Ras pathway to the phenotype induced in PC12 cells by the expression of either Ret-2A or Ret-2B mutants. We show that the Ret-induced molecular and morphological changes are both mediated by Ras-dependent pathways. However, even though inhibition of Ras activity was sufficient to revert Ret-induced differentiation, the kinetics of morphological reversion of the Ret-2B- was more rapid than the Ret-2A- transfected cells. Further, we show that in Ret-transfected cells the suc1- associated neurotrophic factor-induced tyrosine phosphorylation target, SNT, is chronically phosphorylated in tyrosine residues, and associates with the Sos substrate. These results indicate the activation of the Ras cascade as an essential pathway triggered by the chronic active Ret mutants in PC12 cells. Moreover, our data indicate SNT as a substrate for both Ret mutants, which might mediate the activation of this cascade
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