Update frontmatter .md files

pathways/WP23/WP23.md

@@ -1,13 +1,13 @@
 ---
 annotations:
-- id: PW:0000822
-  parent: signaling pathway
-  type: Pathway Ontology
-  value: B cell receptor signaling pathway
 - id: PW:0000818
   parent: signaling pathway
   type: Pathway Ontology
   value: signaling pathway pertinent to immunity
+- id: PW:0000822
+  parent: signaling pathway
+  type: Pathway Ontology
+  value: B cell receptor signaling pathway
 - id: CL:0000236
   parent: native cell
   type: Cell Type Ontology
@@ -97,15 +97,15 @@ description: 'The functional B-cell receptor is a multi-protein complex consisti
   A. (2010). NetPath: A public resource of curated signal transduction pathways. <i>Genome
   Biology</i>. 11:R3.  Proteins on this pathway have targeted assays available via
   the [https://assays.cancer.gov/available_assays?wp_id=WP23 CPTAC Assay Portal]'
-last-edited: 2024-09-22
+last-edited: 2024-09-23
 ndex: 6ec414d7-8b5f-11eb-9e72-0ac135e8bacf
 organisms:
 - Homo sapiens
 redirect_from:
 - /index.php/Pathway:WP23
 - /instance/WP23
-- /instance/WP23_r135522
-revision: r135522
+- /instance/WP23_r135532
+revision: r135532
 schema-jsonld:
 - '@context': https://schema.org/
   '@id': https://wikipathways.github.io/pathways/WP23.html

pathways/WP2846/WP2846.md

@@ -1,17 +1,17 @@
 ---
 annotations:
-- id: CL:0000182
-  parent: native cell
-  type: Cell Type Ontology
-  value: hepatocyte
-- id: PW:0001304
-  parent: classic metabolic pathway
-  type: Pathway Ontology
-  value: cholesterol metabolic pathway
 - id: PW:0000482
   parent: classic metabolic pathway
   type: Pathway Ontology
   value: lipoprotein metabolic pathway
+- id: PW:0001304
+  parent: classic metabolic pathway
+  type: Pathway Ontology
+  value: cholesterol metabolic pathway
+- id: CL:0000182
+  parent: native cell
+  type: Cell Type Ontology
+  value: hepatocyte
 authors:
 - Susan
 - MaintBot
@@ -31,15 +31,15 @@ description: 'Exogenously, circulating PCSK9 (Proprotein convertase subtilisin/k
   the cell surface, leading it to lysosomal degradation. However, the precise mechanisms
   by which the intrinsic degradation pathway operates are still unknown. Abbreviations:
   LDLR, LDL receptor; PCSK9, proprotein convertase subtilisin/kexin type 9.'
-last-edited: 2024-08-09
+last-edited: 2024-09-23
 ndex: c467644c-8b65-11eb-9e72-0ac135e8bacf
 organisms:
 - Homo sapiens
 redirect_from:
 - /index.php/Pathway:WP2846
 - /instance/WP2846
-- /instance/WP2846_r135221
-revision: r135221
+- /instance/WP2846_r135533
+revision: r135533
 schema-jsonld:
 - '@context': https://schema.org/
   '@id': https://wikipathways.github.io/pathways/WP2846.html

pathways/WP4522/WP4522.md

@@ -1,57 +1,57 @@
 ---
 annotations:
-- id: DOID:13809
+- id: DOID:0090105
   parent: genetic disease
   type: Disease Ontology
-  value: familial combined hyperlipidemia
-- id: DOID:0111368
+  value: autosomal recessive hypercholesterolemia
+- id: DOID:1388
   parent: genetic disease
   type: Disease Ontology
-  value: cholesterol-ester transfer protein deficiency
-- id: PW:0000484
-  parent: classic metabolic pathway
-  type: Pathway Ontology
-  value: altered lipoprotein metabolic pathway
-- id: PW:0000153
-  parent: classic metabolic pathway
-  type: Pathway Ontology
-  value: triacylglycerol metabolic pathway
-- id: PW:0000482
-  parent: classic metabolic pathway
-  type: Pathway Ontology
-  value: lipoprotein metabolic pathway
-- id: PW:0000175
-  parent: disease pathway
-  type: Pathway Ontology
-  value: familial combined hyperlipidemia pathway
-- id: DOID:0090105
+  value: Tangier disease
+- id: DOID:13809
   parent: genetic disease
   type: Disease Ontology
-  value: autosomal recessive hypercholesterolemia
+  value: familial combined hyperlipidemia
 - id: PW:0000013
   parent: disease pathway
   type: Pathway Ontology
   value: disease pathway
-- id: DOID:1390
+- id: PW:0000482
+  parent: classic metabolic pathway
+  type: Pathway Ontology
+  value: lipoprotein metabolic pathway
+- id: DOID:1386
   parent: genetic disease
   type: Disease Ontology
-  value: hypobetalipoproteinemia
+  value: abetalipoproteinemia
 - id: DOID:0111418
   parent: genetic disease
   type: Disease Ontology
   value: familial apolipoprotein C-II deficiency
-- id: DOID:1386
+- id: PW:0000175
+  parent: disease pathway
+  type: Pathway Ontology
+  value: familial combined hyperlipidemia pathway
+- id: DOID:1390
   parent: genetic disease
   type: Disease Ontology
-  value: abetalipoproteinemia
-- id: DOID:1388
+  value: hypobetalipoproteinemia
+- id: DOID:0111368
   parent: genetic disease
   type: Disease Ontology
-  value: Tangier disease
+  value: cholesterol-ester transfer protein deficiency
 - id: DOID:14118
   parent: genetic disease
   type: Disease Ontology
   value: familial lipoprotein lipase deficiency
+- id: PW:0000153
+  parent: classic metabolic pathway
+  type: Pathway Ontology
+  value: triacylglycerol metabolic pathway
+- id: PW:0000484
+  parent: classic metabolic pathway
+  type: Pathway Ontology
+  value: altered lipoprotein metabolic pathway
 authors:
 - Ingebude
 - DeSl
@@ -105,15 +105,15 @@ description: 'This pathway shows genetic disorders related to lipoprotein metabo
   on the composition of the various lipoproteins in this pathway are visualised in
   [https://www.wikipathways.org/index.php/Pathway:WP3601].  This pathway was inspired
   by Chapter 43 of the book of Blau (ISBN 3642403360 (978-3642403361)). '
-last-edited: 2024-02-25
+last-edited: 2024-09-23
 ndex: 7644e4be-8b6b-11eb-9e72-0ac135e8bacf
 organisms:
 - Homo sapiens
 redirect_from:
 - /index.php/Pathway:WP4522
 - /instance/WP4522
-- /instance/WP4522_r128956
-revision: r128956
+- /instance/WP4522_r135535
+revision: r135535
 schema-jsonld:
 - '@context': https://schema.org/
   '@id': https://wikipathways.github.io/pathways/WP4522.html
@@ -131,29 +131,28 @@ schema-jsonld:
     are visualised in [https://www.wikipathways.org/index.php/Pathway:WP3601].  This
     pathway was inspired by Chapter 43 of the book of Blau (ISBN 3642403360 (978-3642403361)). '
   keywords:
-  - A-I
-  - A-II
   - ABCA1
-  - Annexin A2
+  - ANXA2
+  - APOA1
+  - APOA2
+  - APOC2
+  - APOE
   - B100
-  - C-II
   - CETP
   - Cholesterol
   - Cyclic fatty acids
-  - E
-  - HL
-  - 'HL '
   - IDL
   - LCAT
   - LDL
-  - LDL-receptor
   - LDLR
   - LDLRAP1
+  - LIPC
+  - LIPG
   - LPL
   - MTP
   - PCSK9
   - Remnant receptor
-  - SR-B1
+  - SCARB1
   - VLDL
   - apo B-48
   license: CC0