From d02c4be6385f7572fb22badc03aba67757bdd14a Mon Sep 17 00:00:00 2001 From: Glass Date: Wed, 29 Nov 2023 13:51:38 -0700 Subject: [PATCH] update resource fixture (#488) Fixes duplicated descriptions --- frontend/src/pages/resources/resources.json | 22 ++++++++++----------- 1 file changed, 11 insertions(+), 11 deletions(-) diff --git a/frontend/src/pages/resources/resources.json b/frontend/src/pages/resources/resources.json index 677d088d0..3e300340e 100644 --- a/frontend/src/pages/resources/resources.json +++ b/frontend/src/pages/resources/resources.json @@ -1,13 +1,13 @@ { "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" @@ -15,19 +15,19 @@ ], "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" @@ -35,37 +35,37 @@ ], "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"