diff --git a/pathways/WP241/WP241.md b/pathways/WP241/WP241.md
index ee891dc871..44d234a892 100644
--- a/pathways/WP241/WP241.md
+++ b/pathways/WP241/WP241.md
@@ -21,6 +21,7 @@ authors:
 - DeSl
 - Fehrhart
 - Eweitz
+- Ddigles
 citedin:
 - link: PMC4127987
   title: Polymorphisms in genes related to one-carbon metabolism are not related to
@@ -50,15 +51,15 @@ description: 'This one-carbon metabolism pathway is centered around folate. Fola
   (vitamin B9) and of methionine.   Proteins on this pathway have targeted assays
   available via the [https://assays.cancer.gov/available_assays?wp_id=WP241 CPTAC
   Assay Portal]'
-last-edited: 2022-01-29
+last-edited: 2023-07-18
 ndex: 4f5ee643-8b61-11eb-9e72-0ac135e8bacf
 organisms:
 - Homo sapiens
 redirect_from:
 - /index.php/Pathway:WP241
 - /instance/WP241
-- /instance/WP241_r120901
-revision: r120901
+- /instance/WP241_r126998
+revision: r126998
 schema-jsonld:
 - '@context': https://schema.org/
   '@id': https://wikipathways.github.io/pathways/WP241.html
diff --git a/pathways/WP4806/WP4806.md b/pathways/WP4806/WP4806.md
index c3022f2bde..611a9e61ac 100644
--- a/pathways/WP4806/WP4806.md
+++ b/pathways/WP4806/WP4806.md
@@ -1,17 +1,17 @@
 ---
 annotations:
-- id: PW:0000298
+- id: PW:0001195
   parent: signaling pathway
   type: Pathway Ontology
-  value: altered growth factor signaling pathway
+  value: tyrosine-specific protein kinase mediated signaling pathway
 - id: PW:0001537
   parent: signaling pathway
   type: Pathway Ontology
   value: altered tyrosine-specific protein kinase mediated signaling pathway
-- id: PW:0001195
+- id: PW:0000298
   parent: signaling pathway
   type: Pathway Ontology
-  value: tyrosine-specific protein kinase mediated signaling pathway
+  value: altered growth factor signaling pathway
 authors:
 - Khanspers
 - Egonw
@@ -33,15 +33,17 @@ description: Tyrosine kinase inhibitors (TKIs) are drugs that inhibit the phosph
   binds to the EGF-family of ligands. It activates several downstream signaling cascades,
   including MAPK, and leads to DNA synthesis and cell proliferation. Mutations and
   over-expression in EGFR is implicated in many cancers.  The section of the pathway
-  outlined in pink corresponds to mechanisms of TKI resistance.
-last-edited: 2021-05-14
+  outlined in pink corresponds to mechanisms of TKI resistance.  This pathway was
+  based on [https://www.kegg.jp/kegg-bin/show_pathway?hsa01521 KEGG].
+last-edited: 2023-07-18
 ndex: 825693c1-8b6d-11eb-9e72-0ac135e8bacf
 organisms:
 - Homo sapiens
 redirect_from:
 - /index.php/Pathway:WP4806
 - /instance/WP4806
-revision: null
+- /instance/WP4806_r127006
+revision: r127006
 schema-jsonld:
 - '@context': https://schema.org/
   '@id': https://wikipathways.github.io/pathways/WP4806.html
@@ -57,14 +59,14 @@ schema-jsonld:
     kinase that binds to the EGF-family of ligands. It activates several downstream
     signaling cascades, including MAPK, and leads to DNA synthesis and cell proliferation.
     Mutations and over-expression in EGFR is implicated in many cancers.  The section
-    of the pathway outlined in pink corresponds to mechanisms of TKI resistance.
+    of the pathway outlined in pink corresponds to mechanisms of TKI resistance.  This
+    pathway was based on [https://www.kegg.jp/kegg-bin/show_pathway?hsa01521 KEGG].
   keywords:
   - AKT1
   - AKT2
   - AKT3
   - ARAF
   - AXL
-  - Apoptosis
   - BAD
   - BAX
   - BCL2
@@ -81,7 +83,6 @@ schema-jsonld:
   - EIF4EBP1
   - ERBB2
   - ERBB3
-  - Epitheial-Mesenchymal Transition
   - Erlotinib
   - FGF2
   - FGFR2
diff --git a/pathways/WP5345/WP5345.md b/pathways/WP5345/WP5345.md
index d83ae2f1af..22f8aac00a 100644
--- a/pathways/WP5345/WP5345.md
+++ b/pathways/WP5345/WP5345.md
@@ -1,13 +1,13 @@
 ---
 annotations:
-- id: DOID:0060410
-  parent: genetic disease
-  type: Disease Ontology
-  value: chromosome 1p36 deletion syndrome
 - id: PW:0000013
   parent: disease pathway
   type: Pathway Ontology
   value: disease pathway
+- id: DOID:0060410
+  parent: genetic disease
+  type: Disease Ontology
+  value: chromosome 1p36 deletion syndrome
 authors:
 - KieranReidy
 - ElenaDR1
@@ -23,14 +23,14 @@ communities:
 - RareDiseases
 description: 1p36 deletion syndrome is a rare genetic disorder caused by the deletion
   of the most distal light band of the short arm of chromosome 1.
-last-edited: 2023-07-10
+last-edited: 2023-07-18
 organisms:
 - Homo sapiens
 redirect_from:
 - /index.php/Pathway:WP5345
 - /instance/WP5345
-- /instance/WP5345_r126967
-revision: r126967
+- /instance/WP5345_r127005
+revision: r127005
 schema-jsonld:
 - '@context': https://schema.org/
   '@id': https://wikipathways.github.io/pathways/WP5345.html