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    <original_author id="date">2019-03-19</original_author>
    <original_author id="name">Cecilia Mascia</original_author>
    <original_author id="organisation">CRS4, Italy</original_author>
    <original_author id="email">cecilia.mascia@crs4.it</original_author>
    <other_contributors>Vebjørn Arntzen, Oslo University Hospital, Norway (openEHR Editor)</other_contributors>
    <other_contributors>Silje Ljosland Bakke, Helse Vest IKT AS, Norway (openEHR Editor)</other_contributors>
    <other_contributors>SB Bhattacharyya, Sudisa Consultancy Services, India</other_contributors>
    <other_contributors>Francesca Frexia, CRS4 - Center for advanced studies, research and development in Sardinia, Italy</other_contributors>
    <other_contributors>Gideon Giacomelli, Charité Berlin, Germany</other_contributors>
    <other_contributors>Heather Grain, Llewelyn Grain Informatics, Australia</other_contributors>
    <other_contributors>Evelyn Hovenga, EJSH Consulting, Australia</other_contributors>
    <other_contributors>Christina Jaeger-Schmidt, Heidelberg University Hospital, Germany</other_contributors>
    <other_contributors>Florian Kaercher, Charité Berlin, Germany</other_contributors>
    <other_contributors>Heather Leslie, Atomica Informatics, Australia (openEHR Editor)</other_contributors>
    <other_contributors>Cecilia Mascia, CRS4, Italy (openEHR Editor)</other_contributors>
    <other_contributors>Ian McNicoll, freshEHR Clinical Informatics, United Kingdom (openEHR Editor)</other_contributors>
    <other_contributors>Andrej Orel, Marand d.o.o., Slovenia</other_contributors>
    <other_contributors>Simon Schumacher, HiGHmed, Germany</other_contributors>
    <other_contributors>Natalia Strauch, Medizinische Hochschule Hannover, Germany</other_contributors>
    <other_contributors>Nyree Taylor, Ocean Informatics, Australia</other_contributors>
    <other_contributors>Aurelie Tomczak, Uniklinikum Heidelberg, Germany (openEHR Editor)</other_contributors>
    <other_contributors>Paolo Uva, CRS4, Italy</other_contributors>
    <other_contributors>Gianluigi Zanetti, CRS4, Italy</other_contributors>
    <lifecycle_state>published</lifecycle_state>
    <other_details id="licence">This work is licensed under the Creative Commons Attribution-ShareAlike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-sa/4.0/.</other_details>
    <other_details id="custodian_organisation">openEHR Foundation</other_details>
    <other_details id="original_namespace">org.openehr</other_details>
    <other_details id="original_publisher">openEHR Foundation</other_details>
    <other_details id="custodian_namespace">org.openehr</other_details>
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      <language>
        <terminology_id>
          <value>ISO_639-1</value>
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        <code_string>de</code_string>
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      <purpose>Zur Darstellung einer Referenz auf eine Wissensdatenbank und / oder auf in der Wissensdatenbank enthaltene Elemente in Bezug auf bestimmte Informationen zu Gesundheitsakten, die diese Wissensdatenbanken verwenden.</purpose>
      <keywords>Pipeline, Datenbank, Analysetool, Software, Wissensdatenbank, Bibliothek</keywords>
      <use>Verwenden Sie diesen Archetyp, um einen Verweis auf eine Wissensdatenbank und / oder auf in der Wissensdatenbank enthaltene Elemente in Bezug auf bestimmte Informationen zu Gesundheitsakten aufzuzeichnen, die diese Wissensdatenbank verwenden.&#xD;
&#xD;
Dieser Archetyp soll, wenn klinisch angemessen, in andere ENTRY- oder CLUSTER-Archetypen verschachtelt werden. Beispielsweise kann er innerhalb des Archetyps CLUSTER.genomic_variant_result an einer von drei Stellen verwendet werden, um Details zum "Bioinformatics analysis workflow","Predicted impact analysis" und "Population allele frequency" darzustellen.</use>
      <misuse>Darf nicht verwendet werden, um tatsächliche Informationen zu replizieren, die in einer Wissensdatenbank enthalten sind.</misuse>
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        <terminology_id>
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        <code_string>nb</code_string>
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      <purpose>For å registrere en referanse til en kunnskapsbase, og/eller til elementer som finnes i kunnskapsbasen, og der innholdet i kunnskapsbasen er relevant for informasjonen som er registrert i pasientjournalen.</purpose>
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      <keywords>pipeline</keywords>
      <keywords>database</keywords>
      <keywords>analyse verktøy</keywords>
      <keywords>software</keywords>
      <keywords>programvare</keywords>
      <keywords>arbeidsflytverktøy</keywords>
      <keywords>bioinformatikk</keywords>
      <keywords>knowledgebase</keywords>
      <use>Brukes for å registrere en referanse til en kunnskapsbase, og/eller til elementer som finnes i kunnskapsbasen, og der innholdet i kunnskapsbasen er relevant for informasjonen som er registrert i pasientjournalen.&#xD;
&#xD;
Denne arketypen er ment å være nøstet i andre ENTRY- eller CLUSTER-arketyper hvor det er klinisk hensiktsmessig. For eksempel kan den brukes i i arketypen CLUSTER.genomic_variant_result (Genetisk variant resultat) flere steder - for eksempel: for å registrere detaljer om arbeidsflyten for 'Bioinformatisk pipeline (Bioinformatics analysis workflow); 'Predikert betydning (Predicted impact analysis)'; og 'Populasjonsallelfrekvens detaljer (Population allele frequency details)'.</use>
      <misuse>Skal ikke brukes til å gjengi faktisk informasjon i en kunnskapsbase.</misuse>
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          <value>ISO_639-1</value>
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        <code_string>en</code_string>
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      <purpose>To record a reference to a knowledge base, and/or to items contained within the knowledge base, in relation to specific health record information which uses that knowledge base.</purpose>
      <keywords>pipeline, database, analysis tool, software, knowledgebase, library</keywords>
      <use>Use to record a reference to a knowledge base, and/or to items contained within the knowledge base, in relation to specific health record information which uses that knowledge base.&#xD;
&#xD;
This archetype is intended to be nested within other ENTRY or CLUSTER archetypes, as clinically appropriate. For example, it may be used within the CLUSTER.genomic_variant_result archetype in one of three places - to record details about the 'Bioinformatics analysis workflow'; 'Predicted impact analysis'; and 'Population allele frequency'.</use>
      <misuse>Not to be used to replicate actual information contained within a knowledge base.</misuse>
      <copyright>© openEHR Foundation</copyright>
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    <author id="name">Aurelie Tomczak, Natalia Strauch</author>
    <author id="organisation">Institute of Pathology, University Hospital Heidelberg, Medizinische Hochschule Hannover</author>
    <author id="email">au.tomczak@yahoo.com, Strauch.Natalia@mh-hannover.de</author>
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    <author id="name">Liv Laugen</author>
    <author id="organisation">​Oslo University Hospital, Norway</author>
    <author id="email">liv.laugen@ous-hf.no</author>
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        <items id="description">A citation of a digital resource used as an source of authoritative or expert information, and/or to items contained within the resource.</items>
        <items id="comment">For example: a genomics pipeline history, a database of genomic variants, or a database of healthcare procedure guidelines.</items>
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        <items id="description">The name of the knowledge base.</items>
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        <items id="text">Item version</items>
        <items id="description">The version of the referenced item within the knowledge base.</items>
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        <items id="description">The hyperlink to the referenced item within the knowledge base.</items>
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        <items id="description">Additional narrative about the knowledge base, not captured in other fields.</items>
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        <items id="text">Item name</items>
        <items id="description">The name of the referenced item within the knowledge base.</items>
        <items id="comment">For example: rs139581412.</items>
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        <items id="text">Knowledge base version</items>
        <items id="description">The version of the referenced knowledge base.</items>
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        <items id="text">Item publication</items>
        <items id="description">Date and/or time when the item within the database was published.</items>
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        <items id="text">Knowledge base URI</items>
        <items id="description">The hyperlink to the referenced knowledge base.</items>
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        <items id="text">Knowledge base reference</items>
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        <items id="comment">For example: a genomics pipeline history, a database of genomic variants, or a database of healthcare procedure guidelines.</items>
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      <items code="at0001">
        <items id="text">Knowledge base name</items>
        <items id="description">The name of the knowledge base.</items>
        <items id="comment">For example: Galaxy/Snakemake; dbSNP; or CADD.</items>
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      <items code="at0002">
        <items id="text">Item version</items>
        <items id="description">The version of the referenced item within the knowledge base.</items>
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      <items code="at0003">
        <items id="text">Item URI</items>
        <items id="description">The hyperlink to the referenced item within the knowledge base.</items>
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      <items code="at0004">
        <items id="text">Comment</items>
        <items id="description">Additional narrative about the knowledge base, not captured in other fields.</items>
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      <items code="at0005">
        <items id="text">Item name</items>
        <items id="description">The name of the referenced item within the knowledge base.</items>
        <items id="comment">For example: rs139581412.</items>
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      <items code="at0006">
        <items id="text">Knowledge base version</items>
        <items id="description">The version of the referenced knowledge base.</items>
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      <items code="at0007">
        <items id="text">Item publication</items>
        <items id="description">Date and/or time when the item within the database was published.</items>
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      <items code="at0008">
        <items id="text">Knowledge base URI</items>
        <items id="description">The hyperlink to the referenced knowledge base.</items>
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        <items id="comment">For eksempel: en tidligere publisert genomisk pipeline, en databaseoppføring med genomiske varianter eller en database med retningslinjer/prosedyrer for/i helsevesenet.</items>
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        <items id="comment">For eksempel: Galaxy/Snakemake; dbSNP; eller CADD.</items>
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        <items id="description">Versjonen til det refererte elementet i kunnskapsbasen.</items>
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      <items code="at0003">
        <items id="text">Element URL</items>
        <items id="description">Hyperlinken til det refererte elementet i kunnskapsbasen.</items>
      </items>
      <items code="at0004">
        <items id="text">Kommentar</items>
        <items id="description">Tekstlig tilleggsinformasjon om kunnskapsbasen som ikke er fanget opp i andre felter.</items>
      </items>
      <items code="at0005">
        <items id="text">Elementnavn</items>
        <items id="description">Navnet på det refererte elementet i kunnskapsbasen.</items>
        <items id="comment">For eksempel: rs139581412.</items>
      </items>
      <items code="at0006">
        <items id="text">Kunnskapsbasens versjon</items>
        <items id="description">Versjonen til kunnskapsbasen/ressursen.</items>
      </items>
      <items code="at0007">
        <items id="text">Element publikasjon</items>
        <items id="description">Dato og/eller klokkeslett da elementet i databasen ble publisert.</items>
      </items>
      <items code="at0008">
        <items id="text">Kunnskapsbase URL</items>
        <items id="description">En hyperlink til den refererte kunnskapsbasen.</items>
      </items>
    </term_definitions>
  </ontology>
</archetype>
