RDF Feed

Normally for an RSS Feed you would use the below script to display the title and link of a given article. But what if I was working with an RDF Feed? Both come from a Feed Block.

------------------- XML (RSS Feed Script) ---------------------

#set($channel = $_XPathTool.selectNodes($contentRoot, '//channel/item'))
#set($title = $channel.getChild("title").text)
#set ($count = 1)

<div id="top-right" style="margin-top: 0px;">
<h3>TSRI News</h3>
#foreach ($item in $channel)
#set($title = $item.getChild("title").text)
#set($link = $item.getChild("link").text.replace("&amp;","&"))#set($link = $item.getChild("link").text.replace("&","&amp;"))
    #if($count <= 5)
        <p style="font-size: 75%; padding-left:5px;"><strong>${title}</strong></p>
    <p style="font-size: 75%; padding-left:5px;"><a href="${link}">more</a></p>
    #set($count = $count + 1)
#end
#end
</div>

------------------- RDF (Feed Block) ---------------------

<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:j.0="http://vitro.mannlib.cornell.edu/ns/vitro/public#" xmlns:j.1="http://xmlns.com/foaf/0.1/" xmlns:j.2="http://vivoweb.org/ontology/core#" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#">
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<j.2:researchOverview>&lt;p>Synthetic Organic and Bioorganic Chemistry&lt;/p>&lt;p>Our research interests include the total synthesis of natural  products, development of new synthetic methodology, heterocyclic  chemistry, bioorganic and medicinal chemistry, the study of DNA-agent  interactions, and the chemistry of antitumor antibiotics. We place  special emphasis on investigations to define the structure-function  relationships of natural or designed agents.&lt;/p>&lt;p>Synthetic Methodology&lt;/p>&lt;p>Our ongoing investigations emphasize the development and application  of hetero Diels-Alder reactions, the thermal reactions of cyclopropenone  ketals, inter- and intramolecular acyl radical-alkene addition  reactions, medium and large ring cyclization procedures, and  combinatorial chemistry. In each instance, the methodology development  represents the investigation of chemistry projected as a key step in the  total synthesis of a natural or nonnatural product.&lt;/p>&lt;p>Natural Products Total Synthesis&lt;/p>&lt;p>Problems recently or currently being addressed include (+)-CC-1065  and functional analogs (antitumor antibiotic processing sequence  selective DNA alkylation properties), duocarmycins (antitumor  antibiotics possessing sequence selective DNA alkylation properties),  yatakemycin, tropoloalkaloids, deoxybouvardin/bouvardin, K-13, OF4949-1 -  OF4949-IV (immunopotentiating agents with confirmed antitumor  activity), piperazinomycin, luzopeptins, sandramycin quinoxapeptins,  thiocoraline and BE 22179, (DNA binding peptides with antitumor and  antiviral properties), vancomycin, teicoplanin, chloropeptins, RP-66453,  ramoplanin, bleomycin A2 (clinically employed antitumor agent),  quinolinequinone antitumor antibiotics including streptonigrone,  streptonigrin, and lavendamycin, isochrysohermidin, fredericamycin A and  CI-920 (antitumor agents with topoisomerase I and II inhibitory  activity), rhizoxin (antitumor antibiotic and potent mitotic inhibitor),  combretastatins, and trikentrin A.&lt;/p>&lt;p>Bioorganic Chemistry&lt;/p>&lt;p>The orgin of interest in the specific agents detailed above rests  with their properties and in many instances represents the selection of  agents related by a projected property (e.g., (+)-CC-1065 and  duocarmycin). Representatives of such efforts, studies on (+)-CC-1065  have been employed to identify agent structural features contributing to  its sequence-selective DNA alkylation properties and the source of  catalysis of the DNA alkylation reaction. Efforts are under way to  develop DNA cross-linking agents of a predefined cross-link, to further  understand the nature of the covalent and noncovalent agent-DNA  interactions, and to apply this understanding to the de novo design of  DNA-binding agents.&amp;nbsp;&lt;br />&lt;br />Collaborative efforts in securing biological  data, 1H NMR of DNA-agent complexes, molecular modeling studies of  large molecule-small molecule interactions, and experimental studies of  DNA-agent interactions constitute an integral part of the program.&lt;/p></j.2:researchOverview>
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<j.2:overview>Dr. Dale Boger works on the total synthesis of biologically active natural products using the tools of organic synthesis to identify, imitate, understand, exploit, and sometimes surpass what nature provides.</j.2:overview>
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<rdfs:label xml:lang="en-US">Boger, Dale</rdfs:label>
<j.2:email>[email blocked]</j.2:email>
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