Femke Kramer, Mooi vies, knap lelijk. Grotesk realisme in rederijkerskluchten
نویسندگان
چکیده
منابع مشابه
A Response to Mooi, Williams and Gill
EDWARD O. WILEY, PROSANTA CHAKRABARTY, MATTHEW T. CRAIG, MATTHEW P. DAVIS, NANCY I. HOLCROFT, RICHARD L. MAYDEN & WM. LEO SMITH Department of Ecology and Evolutionary Biology and Biodiversity Research Center, University of Kansas, Lawrence, KS, U.S.A. E-mail: [email protected] Museum of Natural Science, Louisiana State University, Baton Rouge, LA, U.S.A. E-mails: [email protected] (PC), matthewdavis...
متن کاملStructural Stefan Kramer
In many real-world domains the task of machine learning algorithms is to learn a theory for predicting numerical values. In particular several standard test domains used in Inductive Logic Programming (ILP) are concerned with predicting numerical values from examples and relational and mostly non-determinate background knowledge. However, so far no ILP algorithm except one can predict numbers a...
متن کاملOn Kramer-Mesner matrix partitioning conjecture
In 1977, Ganter and Teirlinck proved that any 2t× 2t matrix with 2t nonzero elements can be partitioned into four submatrices of order t of which at most two contain nonzero elements. In 1978, Kramer and Mesner conjectured that any mt× nt matrix with kt nonzero elements can be partitioned into mn submatrices of order t of which at most k contain nonzero elements. In 1995, Brualdi et al. showed ...
متن کامل"Vreselijk mooi!" (terribly beautiful): A Subjectivity Lexicon for Dutch Adjectives
We present a new open source subjectivity lexicon for Dutch adjectives. The lexicon is a dictionary of 1,100 adjectives that occur frequently in online product reviews, manually annotated with polarity strength, subjectivity and intensity, for each word sense. We discuss two machine learning methods (using distributional extraction and synset relations) to automatically expand the lexicon to 5,...
متن کاملStefan Kramer and Neil Lawrence ( Eds . ) Machine Learning in
Variation in human DNA sequences account for a significant amount of genetic risk factors for common disease such as hypertension, diabetes, Alzheimer’s disease, and cancer. Identifying the human sequence variation that makes up the genetic basis of common disease will have a tremendous impact on medicine in many ways. Recent efforts to identify these genetic factors through large scale associa...
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ژورنال
عنوان ژورنال: BMGN - Low Countries Historical Review
سال: 2010
ISSN: 2211-2898,0165-0505
DOI: 10.18352/bmgn-lchr.7148