Strategic refinement: typos (#6958)

- updated typos in comments
- reran normalization (just to make sure)

src/ontology/mondo-edit.obo

@@ -111022,7 +111022,7 @@ replaced_by: MONDO:0018666
 id: MONDO:0006243
 name: hepatoid adenocarcinoma
 def: "An adenocarcinoma with morphologic characteristics similar to hepatocellular carcinoma, arising from an anatomic site other than the liver." [NCIT:C66950]
-comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'MONDO:0004335' (digestive system disorder) ontology branch (https://orcid.org/0000-0001-9310-0163)
+comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'digestive system disorder' (MONDO:0004335) ontology branch (https://orcid.org/0000-0001-9310-0163)
 synonym: "hepatoid adenocarcinoma" EXACT [NCIT:C66950]
 synonym: "hepatoid carcinoma" EXACT [NCIT:C66950]
 xref: DOID:0060534 {source="MONDO:equivalentTo"}
@@ -143544,7 +143544,7 @@ is_a: MONDO:0003847 {source="https://orcid.org/0000-0001-5208-3432"} ! hereditar
 id: MONDO:0007856
 name: palmoplantar keratoderma-esophageal carcinoma syndrome
 def: "An inherited condition characterized by palmoplantar keratoderma and esophageal cancer. The palmoplantar keratoderma usually begins around age 10, and esophageal cancer may form after age 20. This condition is caused by a mutation in the RHBDF2 gene and is inherited in an autosomal dominant pattern." [GARD:0003102, https://orcid.org/0000-0001-5208-3432]
-comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'MONDO:0004335' (digestive system disorder) ontology branch (https://orcid.org/0000-0001-9310-0163)
+comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'digestive system disorder' (MONDO:0004335) ontology branch (https://orcid.org/0000-0001-9310-0163)
 subset: gard_rare
 subset: ordo_disease {source="Orphanet:2198"}
 synonym: "Bennion-Patterson syndrome" EXACT [Orphanet:2198]
@@ -145181,7 +145181,7 @@ property_value: seeAlso "https://rarediseases.info.nih.gov/diseases/147/macrocep
 id: MONDO:0007924
 name: Bannayan-Riley-Ruvalcaba syndrome
 def: "Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare congenital disorder characterized by hamartomatous intestinal polyposis, lipomas, macrocephaly and genital lentiginosis." [Orphanet:109]
-comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'MONDO:0004335' (digestive system disorder) ontology branch (https://orcid.org/0000-0001-9310-0163)
+comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'digestive system disorder' (MONDO:0004335) ontology branch (https://orcid.org/0000-0001-9310-0163)
 subset: gard_rare {source="GARD:0005887"}
 subset: ordo_malformation_syndrome {source="Orphanet:109"}
 synonym: "Bannayan syndrome" EXACT [NCIT:C3939]
@@ -170131,7 +170131,7 @@ property_value: seeAlso "https://rarediseases.info.nih.gov/diseases/6233/cystic-
 id: MONDO:0009062
 name: cystic fibrosis-gastritis-megaloblastic anemia syndrome
 def: "A rare genetic disease reported in two siblings of consanguineous Arab parents and is characterized by cystic fibrosis, gastritis associated with Helicobacter pylori, folate deficiency megaloblastic anemia, and intellectual disability. There have been no further descriptions in the literature since 1991." [Orphanet:2575]
-comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'MONDO:0004335' (digestive system disorder) ontology branch (https://orcid.org/0000-0001-9310-0163)
+comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'digestive system disorder' (MONDO:0004335) ontology branch (https://orcid.org/0000-0001-9310-0163)
 subset: ordo_disease {source="Orphanet:2575"}
 synonym: "cystic fibrosis gastritis megaloblastic anaemia" RELATED OMO:0003005 []
 synonym: "cystic fibrosis gastritis megaloblastic anemia" RELATED [GARD:0003303]
@@ -174164,7 +174164,7 @@ relationship: disease_has_infectious_agent NCBITaxon:173087 ! Human papillomavir
 id: MONDO:0009238
 name: hereditary folate malabsorption
 def: "Hereditary folate malabsorption (HFM) is an inherited disorder of folate transport characterized by a systemic and central nervous system (CNS) folate deficiency manifesting as megaloblastic anemia, failure to thrive, diarrhea and/or oral mucositis, immunologic dysfunction and neurological disorders." [Orphanet:90045]
-comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'MONDO:0004335' (digestive system disorder) ontology branch (https://orcid.org/0000-0001-9310-0163)
+comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'digestive system disorder' (MONDO:0004335) ontology branch (https://orcid.org/0000-0001-9310-0163)
 subset: gard_rare {source="GARD:0012983"}
 subset: ordo_disease {source="Orphanet:90045"}
 synonym: "congenital defect of folate absorption" RELATED [GARD:0012983]
@@ -288510,7 +288510,7 @@ property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/
 [Term]
 id: MONDO:0014421
 name: glucocorticoid resistance
-comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'https://github.com/monarch-initiative/mondo/issues/6753' (MONDO:0005039) ontology branch (https://orcid.org/0000-0001-9310-0163|https://orcid.org/0000-0002-2825-0621)
+comment: This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'reproductive system disorder' (MONDO:0005039) ontology branch (https://orcid.org/0000-0001-9310-0163|https://orcid.org/0000-0002-2825-0621)
 subset: gard_rare {source="GARD:0002499"}
 subset: ordo_disease {source="Orphanet:786"}
 synonym: "cortisol resistance from glucocorticoid receptor defect" RELATED [OMIM:615962]