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A bibliographic record is an entry in a bibliographic index (or a library catalog) which represents and describes a specific resource.A bibliographic record contains the data elements necessary to help users identify and retrieve that resource, as well as additional supporting information, presented in a formalized bibliographic format.
The RIS file format—two letters, two spaces and a hyphen—is a tagged format for expressing bibliographic citations.According to the specifications, [3] [4] [5] the lines must end with the ASCII carriage return and line feed characters.
This example is the most basic and includes unique references for each citation, showing the page numbers in the reference list. This repeats the citation, changing the page number. A disadvantage is that this can create a lot of redundant text in the reference list when a source is cited many times. So consider using one of the alternatives ...
Group 3 entities are subjects of Group 1 or Group 2’s intellectual endeavor, and include concepts, objects, events, and places. Group 1 entities. Group 1 entities are the foundation of the FRBR model: Work is a "distinct intellectual or artistic creation." [3] For example, Beethoven's Ninth Symphony apart from all ways of expressing it is a ...
MARC 21 was designed to redefine the original MARC record format for the 21st century and to make it more accessible to the international community. MARC 21 has formats for the following five types of data: Bibliographic Format, Authority Format, Holdings Format, Community Format, and Classification Data Format. [3]
HTML Form format HTML 4.01 Specification since PDF 1.5; HTML 2.0 since 1.2 Forms Data Format (FDF) based on PDF, uses the same syntax and has essentially the same file structure, but is much simpler than PDF since the body of an FDF document consists of only one required object. Forms Data Format is defined in the PDF specification (since PDF 1.2).
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A case report form (or CRF) is a paper or electronic questionnaire specifically used in clinical trial research. [1] The case report form is the tool used by the sponsor of the clinical trial to collect data from each participating patient.