<bold>

Bold

Used to mark text that should appear in bold face.

Attribute

specific-use Specific Use

Content Model

<!ELEMENT  bold         (#PCDATA %emphasized-text;)*                 >

Expanded Content Model

(#PCDATA | email | ext-link | uri | inline-supplementary-material | related-article | related-object | bold | italic | monospace | overline | roman | sans-serif | sc | strike | underline | alternatives | inline-graphic | private-char | chem-struct | inline-formula | tex-math | mml:math | abbrev | milestone-end | milestone-start | named-content | styled-content | fn | target | xref | sub | sup)*

Description

Any combination of:

This element may be contained in:

<addr-line>, <aff>, <alt-title>, <article-title>, <attrib>, <award-id>, <bold>, <chapter-title>, <chem-struct>, <collab>, <comment>, <compound-kwd-part>, <compound-subject-part>, <conf-theme>, <copyright-statement>, <corresp>, <def-head>, <disp-formula>, <element-citation>, <ext-link>, <funding-source>, <funding-statement>, <gov>, <inline-formula>, <inline-supplementary-material>, <italic>, <kwd>, <label>, <license-p>, <meta-value>, <mixed-citation>, <monospace>, <named-content>, <on-behalf-of>, <overline>, <p>, <part-title>, <preformat>, <price>, <product>, <related-article>, <related-object>, <role>, <roman>, <sans-serif>, <sc>, <series>, <series-text>, <series-title>, <sig>, <sig-block>, <source>, <std>, <strike>, <styled-content>, <sub>, <subject>, <subtitle>, <sup>, <supplement>, <target>, <td>, <term>, <term-head>, <textual-form>, <th>, <title>, <trans-source>, <trans-subtitle>, <trans-title>, <underline>, <verse-line>, <xref>

Example

...
<p>... The third nucleotide (CG<bold>A</bold>) at codon 529, which
is a specific nucleotide of <italic>M. tuberculosis</italic>
(<xref ref-type="bibr" rid="B8">8</xref>, <xref ref-type="bibr"
rid="B11">11</xref>), was not clearly determined by conventional PCR direct
sequencing. Furthermore, PCR sequencing misidentified codon 531 as
T<bold>C</bold>G, which reflects the rifampin-susceptible strain. However,
the second nucleotide at codon 531, which is the most frequent site of
mutation related to rifampin resistance, was determined as
T<bold>T</bold>G by nested PCR sequencing (Fig. <xref ref-type="fig"
rid="F5">5</xref>, lower panel). ...</p>
...

Module

JATS-format1.ent