Process GPML changes

pathways/WP5502/WP5502.gpml

@@ -1,5 +1,5 @@
 <?xml version="1.0" encoding="UTF-8"?>
-<Pathway xmlns="http://pathvisio.org/GPML/2013a" Name="16p13.11 copy number variation syndrome " Data-Source="WikiPathways" Version="WP5502_r136091" Author="[Alval, Egonw]" Last-Modified="20241215163027" Organism="Homo sapiens">
+<Pathway xmlns="http://pathvisio.org/GPML/2013a" Name="16p13.11 copy number variation syndrome " Data-Source="WikiPathways" Version="WP5502_r136092" Author="[Alval, Egonw]" Last-Modified="20241217203745" Organism="Homo sapiens">
   <Comment Source="WikiPathways-description">Copy number variations in the region 16p13.11 (exact position: chr16:15511655-16293689 (GRCh37), are rare, pathological mutations in the human genome. It is a risk variation for neuropsychiatric diseases like schizophrenia (Kirov et al. 2014, 10.1016/j.biopsych.2013.07.022)</Comment>
   <Attribute Key="org.pathvisio.sbgn.language" Value="process description" />
   <Graphics BoardWidth="1768.1902696850134" BoardHeight="1075.1529645637675" />
@@ -61,7 +61,6 @@
   </DataNode>
   <DataNode TextLabel="MYH11" GraphId="ade83" Type="GeneProduct">
     <Comment>smooth muscle myosin heavy chain (SMMHC)</Comment>
-    <Comment>Type your comment here</Comment>
     <Graphics CenterX="1432.532594729436" CenterY="229.39518503310703" Width="129.39521800281295" Height="20.00000000000004" ZOrder="32923" FontSize="12" Valign="Middle" />
     <Xref Database="Ensembl" ID="ENSG00000133392" />
   </DataNode>
@@ -131,7 +130,6 @@
   </DataNode>
   <DataNode TextLabel="NDE1" GraphId="d76ac" Type="GeneProduct">
     <Comment>NudE Neurodevelopment Protein 1</Comment>
-    <Comment>Type your comment here</Comment>
     <Graphics CenterX="1008.8979067292013" CenterY="229.39518503310708" Width="129.39521800281298" Height="20.000000000000075" ZOrder="32938" FontSize="12" Valign="Middle" />
     <Xref Database="Ensembl" ID="ENSG00000072864" />
   </DataNode>