update resource fixture (#488)

Fixes duplicated descriptions
monarch-initiative · Nov 29, 2023 · d02c4be · d02c4be
1 parent 5d05043
commit d02c4be
Showing 1 changed file with 11 additions and 11 deletions.
diff --git a/frontend/src/pages/resources/resources.json b/frontend/src/pages/resources/resources.json
@@ -1,71 +1,71 @@
 {
   "Standards": [
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "The Phenopacket Schema is an ISO-endorsed open standard for sharing disease and phenotype information.",
       "icon": "resource-phenopackets",
       "link": "http://phenopackets.org/",
       "name": "Phenopackets"
     },
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "SSSOM is a simple metadata standard for describing semantic mappings.",
       "icon": "resource-sssom",
       "link": "https://mapping-commons.github.io/sssom/spec/",
       "name": "SSSOM"
     }
   ],
   "Ontologies": [
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "The HPO provides a standardized vocabulary of phenotypic abnormalities in human disease.",
       "icon": "resource-hpo",
       "link": "https://hpo.jax.org/app/",
       "name": "HPO"
     },
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "The Mondo Disease Ontology aims to harmonizes disease definitions across the world.",
       "icon": "resource-mondo",
       "link": "https://mondo.monarchinitiative.org/",
       "name": "Mondo"
     },
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "uPheno aims to unify the annotation of phenotypes across species.",
       "icon": "resource-upheno",
       "link": "https://obophenotype.github.io/upheno/",
       "name": "uPheno"
     }
   ],
   "Tools": [
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "The Exomiser is a tool for finding potential disease-causing variants in whole-exome or whole-genome sequencing data.",
       "icon": "resource-exomiser",
       "link": "https://hpo.jax.org/app/tools/exomiser",
       "name": "Exomiser"
     },
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "The Monarch App is a web application for exploring the Monarch Knowledge Graph.",
       "icon": "resource-monarch",
       "link": "https://monarch-initiative.github.io/monarch-documentation",
       "name": "Monarch App"
     },
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "LIkelihood Ratio Interpretation of Clinical AbnormaLities performs phenotype-driven prioritization of candidate diseases and genes in the setting of genomic diagnostics.",
       "icon": "lirical",
       "link": "https://thejacksonlaboratory.github.io/LIRICAL/stable/",
       "name": "LIRICAL"
     },
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "OntoGPT is a Python package for extracting structured information from text with large language models (LLMs), instruction prompts, and ontology-based grounding.",
       "icon": "onto-gpt",
       "link": "https://github.com/monarch-initiative/ontogpt",
       "name": "OntoGPT"
     },
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "AI Assisted Ontology Curation.",
       "icon": "curate-gpt",
       "link": "https://curategpt.io/",
       "name": "CurateGPT"
     },
     {
-      "description": "Open and Computable Bioinformation for Phenotypic Data",
+      "description": "SSSOM Mappings collected and curated by the Monarch Initiative.",
       "icon": "resource-monarch",
       "link": "https://github.com/monarch-initiative/monarch-mapping-commons",
       "name": "Monarch Mapping Commons"