Update tsv, md and png files

Author: actions-user

_data/WP1531-datanodes.tsv

@@ -14,7 +14,7 @@ CYP2R1 	GeneProduct	ncbigene:120227	""	ensembl:ENSG00000186104	ncbigene:120227	h
 DHCR7	GeneProduct	ncbigene:1717	""	ensembl:ENSG00000172893	ncbigene:1717	hgnc.symbol:DHCR7	uniprot:A0A804HI25;uniprot:A0A804HL56;uniprot:E9PQ71;uniprot:E9PJ54;uniprot:B4E1K5;uniprot:H0YCS7;uniprot:H0YE57;uniprot:Q9UBM7;uniprot:E9PM00;uniprot:A0A024R5F7;uniprot:A0A8I5KRR9;uniprot:A0A804HJQ7;uniprot:E9PIP9;uniprot:H0YEJ5;uniprot:A0A804HJI8;uniprot:E9PRL8;uniprot:E9PLZ2								
 CYP27A1	GeneProduct	ncbigene:1593	""	ensembl:ENSG00000135929	ncbigene:1593	hgnc.symbol:CYP27A1	uniprot:Q02318;uniprot:F8WD90;uniprot:C9J1K5								
 Vitamin D binding protein	GeneProduct	ncbigene:2638	""	ensembl:ENSG00000145321	ncbigene:2638	hgnc.symbol:GC	uniprot:P02774;uniprot:D6RBJ7;uniprot:D6RF20;uniprot:D6RF35								
-Alpha globulin	GeneProduct	:https://www.wikidata.org/wiki/Q2440935	""												
+Alpha globulin	GeneProduct	wikidata:Q2440935	""												
 RXRB	GeneProduct	ncbigene:6257	""	ensembl:ENSG00000204231	ncbigene:6257	hgnc.symbol:RXRB	uniprot:Q5STP9;uniprot:P28702;uniprot:E9PK75;uniprot:A0A0S2Z570								
 VDR	GeneProduct	ncbigene:7421	""	ensembl:ENSG00000111424	ncbigene:7421	hgnc.symbol:VDR	uniprot:F8VVY8;uniprot:F8VRJ4;uniprot:F8VXQ9;uniprot:A0A5K1VW50;uniprot:F1D8P8;uniprot:F8VPF8;uniprot:P11473								
 CYP24A1	GeneProduct	ncbigene:1591	""	ensembl:ENSG00000019186	ncbigene:1591	hgnc.symbol:CYP24A1	uniprot:Q07973								

_pathways/WP1531.md

@@ -1,31 +1,31 @@
 ---
 annotations:
-- id: DOID:10609
-  type: Disease Ontology
-  value: rickets
-- id: CL:1000497
-  parent: animal cell
-  type: Cell Type Ontology
-  value: kidney cell
 - id: CL:0002620
   parent: animal cell
   type: Cell Type Ontology
   value: skin fibroblast
-- id: PW:0000135
-  parent: classic metabolic pathway
-  type: Pathway Ontology
-  value: metabolic pathway of cofactors, vitamins, nutrients
 - id: PW:0001011
   parent: classic metabolic pathway
   type: Pathway Ontology
   value: vitamin D metabolic pathway
-- id: DOID:10573
-  type: Disease Ontology
-  value: osteomalacia
+- id: CL:1000497
+  parent: animal cell
+  type: Cell Type Ontology
+  value: kidney cell
 - id: CL:0000182
   parent: native cell
   type: Cell Type Ontology
   value: hepatocyte
+- id: DOID:10609
+  type: Disease Ontology
+  value: rickets
+- id: DOID:10573
+  type: Disease Ontology
+  value: osteomalacia
+- id: PW:0000135
+  parent: classic metabolic pathway
+  type: Pathway Ontology
+  value: metabolic pathway of cofactors, vitamins, nutrients
 authors:
 - Evelo
 - Lribeiro
@@ -75,15 +75,15 @@ description: Photochemical synthesis of vitamin D3 (cholecalciferol, D3) occurs
   growth, and immunity. VDR modulates the expression of genes by forming a heterodimer
   complex with retinoid-X-receptors (RXR).  Proteins on this pathway have targeted
   assays available via the [CPTAC Assay Portal](https://assays.cancer.gov/available_assays?wp_id=WP1531).
-last-edited: 2025-03-06
+last-edited: 2025-12-31
 ndex: ee30232e-8b62-11eb-9e72-0ac135e8bacf
 organisms:
 - Homo sapiens
 redirect_from:
 - /index.php/Pathway:WP1531
 - /instance/WP1531
-- /instance/WP1531_r137603
-revision: r137603
+- /instance/WP1531_r142298
+revision: r142298
 schema-jsonld:
 - '@context': https://schema.org/
   '@id': https://wikipathways.github.io/pathways/WP1531.html

_pathways/WP1604.md

@@ -8,18 +8,18 @@ annotations:
   parent: native cell
   type: Cell Type Ontology
   value: hepatocyte
-- id: DOID:2739
-  parent: genetic disease
-  type: Disease Ontology
-  value: Gilbert syndrome
-- id: PW:0000107
-  parent: classic metabolic pathway
-  type: Pathway Ontology
-  value: xenobiotics biodegradation pathway
 - id: PW:0000754
   parent: drug pathway
   type: Pathway Ontology
   value: drug pathway
+- id: PW:0000107
+  parent: classic metabolic pathway
+  type: Pathway Ontology
+  value: xenobiotics biodegradation pathway
+- id: DOID:2739
+  parent: genetic disease
+  type: Disease Ontology
+  value: Gilbert syndrome
 authors:
 - Khanspers
 - AlexanderPico
@@ -62,15 +62,15 @@ description: The principal pathways for the metabolism of codeine occur in the l
   and morphine.  A disease linked to this pathway is Gilbert syndrome (visualised
   in pink), which is characterized by impaired glucuronidation due to a polymorphism
   in the gene encoding UGT1A1.
-last-edited: 2025-11-04
+last-edited: 2025-12-31
 ndex: 508664cc-8b63-11eb-9e72-0ac135e8bacf
 organisms:
 - Homo sapiens
 redirect_from:
 - /index.php/Pathway:WP1604
 - /instance/WP1604
-- /instance/WP1604_r141113
-revision: r141113
+- /instance/WP1604_r142299
+revision: r142299
 schema-jsonld:
 - '@context': https://schema.org/
   '@id': https://wikipathways.github.io/pathways/WP1604.html

_pathways/WP1946.md

@@ -71,15 +71,15 @@ description: 'The Cori cycle is also known as the Lactic acid cycle, and refers
   the cycle cannot be sustained indefinitely. The Cori cycle shifts the metabolic
   burden from the muscles to the liver.  Source: Adapted from [Wikipedia](https://en.wikipedia.org/wiki/Cori_cycle).  Proteins
   on this pathway have targeted assays available via the [CPTAC Assay Portal](https://assays.cancer.gov/available_assays?wp_id=WP1946).'
-last-edited: 2025-07-09
+last-edited: 2025-12-31
 ndex: 67b302d9-8b63-11eb-9e72-0ac135e8bacf
 organisms:
 - Homo sapiens
 redirect_from:
 - /index.php/Pathway:WP1946
 - /instance/WP1946
-- /instance/WP1946_r139861
-revision: r139861
+- /instance/WP1946_r142301
+revision: r142301
 schema-jsonld:
 - '@context': https://schema.org/
   '@id': https://wikipathways.github.io/pathways/WP1946.html