Sentence examples for secondary ids from inspiring English sources

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Gene ontology analyses indicate one biological process with GO ID: 0006952 representing defense response, with two secondary IDs GO: 0002217 GO: 0042829.

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For FBgn IDs present in Dfam data, for which no Flybase entry was found, Flybase's ID Convertor tool (http://flybase.org/static_pages/downloads/IDConv.html) was used to establish the correspondence between the "Secondary ID" present in Dfam and "Current ID" used in the current version of FlyBase, and the data found for either Current ID or Secondary ID was used for a given paralog.

Although only a select few (ID) systems link directly to pathway and ontology annotations [Ensembl, EntrezGene and HMDB (http://www.hmdb.ca)] by default, all secondary ID systems (e.g. Affymetrix, RefSeq, MGI and Symbol) connect to these through relationship tables.

Likewise, both the Current ID or Secondary ID were used to match paralogs with the expression data Fly Atlas [ 39] and to SNP data obtained from DGRP resequencing project [ 40] (annotation_5_46; http://dgrp.gnets.ncsu.edu/webdata).ncsu.edu/webdata

If you do not have one of those forms of ID, you will need two forms of what are called "secondary ID".

After the user chooses the desired mode, the AGI ID fields must be filled: the primary AGI ID field is required for all modes, as is the secondary AGI ID field in the Compare mode.

The KEGG term of "Biosynthesis of secondary metabolites" (ID: sce01110) involves a number of pathways, including carbon metabolism and biosynthesis of amino acids.

For the second gene, the locus identifier becomes a secondary locus ID (associated with the first one), whereby the second gene's name and symbol will become synonyms of the first one.

Of note, no detectable difference in cell surface marker expression profile was observed between the secondary (patients ID 15 and 16) and de novo GBM specimens analyzed (Table 1).

In 1988, MEDLINE curators started to record information pertaining to the registration of several types of biological data in the Secondary Source ID (SI) field of citations.

Therefore, it is now well recognized that immunosuppressive drugs used in transplanted patients may induce immune defects, thus compromising the immune response and facilitating the development of a secondary immunodeficiency (ID) which can ultimately ease cancer onset [ 5].

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