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Table 1. Research paradigms
"... In PAGE 6: ... Each knowledge interest is also associated with a tradition of systems thinking. ( Table1 ) [35, 36, 44, 45, 47] Table 1. Research paradigms ... ..."
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Table 3. CBO of the Paradigms
in Towards a validation process for measuring coupling: integrating axiomatic and empirical approaches.
Table 111. Test Paradigm.
"... In PAGE 10: ... The Boolean test using SAF or delay fault patterns detects the Open Type-3 defect class. The difficult defect classes, Open Type-5 and -6 and Parametric Delay, are listed in Table111 as lt;loo% detected for available test methods having nontarget detection capability. Available methods are variations of delay fault [71,72], BET, fMMAX, and functional test methods.... ..."
Table 1. Paradigm overview.
"... In PAGE 6: ...of trials for free-viewing and template search was the same as in Experiments 1 and 2, and 2 C2 96 trials of oddity search were performed in addition ( Table1 ). Due to the larger amount of trials, Experiment 3 was split in two sessions on consecutive days: blocks 1 through 6 were performed on the first day, blocks 7 through 12 on the second day.... ..."
Table 3 Paradigm Model
Table 4. NE combinations in novel and non-novel sentences
2005
"... In PAGE 4: ...named entities (Table 3); and (2) there are relatively more novel sentences (in percentiles) than non-novel sentences that contain the four particular NE combinational patterns of interest ( Table4 ). Table 3.... ..."
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Table 2 Novel mutations identified
"... In PAGE 6: ...Study of 94 HHT1 families revealed 75 unique mutations; nine previously unreported mutations are described briefly and shown in Table2 with the clinical phenotype of the proband. Supplementary Figure 1 illustrates the position of these mutations on the mRNA diagrams.... In PAGE 7: .... This mutation likely causes skipping of exon 7, leading to a frameshift. The proband, whose father had a pulmonary haemorrhage of unknown cause, presented with epistaxis as the only clinical sign. We identified 4 novel small ENG insertions leading to frameshift mutations ( Table2 ). In family 508, the proband and mother were each diagnosed with PAVMs.... In PAGE 7: ... Novel ACVRL1 mutations Within the ACVRL1 gene we have identified a total of 43 unique mutations in 58 resolved families. Six of these mutations are novel and are listed in Table2 . Detailed descriptions of some of the mutations are listed below.... ..."
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