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<biogps><data><item key="rating_data"><item key="avg_stars">10</item><item key="total">1</item><item key="avg">5</item></item><item key="name">CIViC</item><item key="created">2016-10-29 03:23:59</item><item key="url">https://civic.genome.wustl.edu/links/entrez/{{entrezgene}}</item><item key="lastmodified">2016-10-29 03:30:45</item><item key="usage_data"><item key="layouts">1.0</item><item key="users">1</item></item><item key="popularity">1.0</item><item key="owner"><item key="username">malachig</item><item key="url">/profile/7397/malachig</item><item key="name">Malachi Griffith</item></item><item key="species"><item>human</item></item><item key="shortUrl">civic.genome.wustl.edu</item><item key="id">1238</item><item key="short_description">Clinical Interpretations for Variants in Cancer (www.civicdb.org)</item><item key="role_permission"><item>biogpsusers</item></item><item key="permission_style">public</item><item key="type">iframe</item><item key="options">None</item><item key="tags"><item>annotation</item><item>cancer</item><item>clinical</item><item>interpretations</item><item>variant</item><item>variants</item></item><item key="description">CIViC is an expert crowdsourced knowledgebase for Clinical Interpretation of Variants in Cancer (www.civicdb.org) describing the therapeutic, prognostic, and diagnostic relevance of inherited and somatic variants of all types. CIViC is committed to open source code, open access content, public application programming interfaces (APIs), and provenance of supporting evidence to allow for the transparent creation of current and accurate variant interpretations for use in cancer precision medicine.</item></data></biogps>
