{
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                "affiliation": "The George Washington University",
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                "email": "martin@ebi.ac.uk"
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                "affiliation": "EMBL-EBI-UniProt",
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                "name": "Preethi Vasudev",
                "email": "pvasudev@ebi.ac.uk"
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                "affiliation": "Monarch Initiative - Oregon Health & Science University",
                "contribution": [
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                "name": "Jean-Philippe Gourdine",
                "email": "gourdine@ohsu.edu"
            },
            {
                "affiliation": "Monarch Initiative - Oregon Health & Science University",
                "contribution": [
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                "name": "Melissa Haendel",
                "email": "haendel@ohsu.edu"
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                "affiliation": "The George Washington University",
                "contribution": [
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                "name": "Karina Martinez",
                "email": "karinamartinez@gwu.edu"
            },
            {
                "name": "Jingyue Wu",
                "affiliation": "The George Washington University",
                "contribution": [
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                "email": "jingyue.wu@email.gwu.edu"
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            "OMIM",
            "Congenital Disorders of Glycosylation (CDG)",
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                "name": "make-protein-dataset.py",
                "step_number": 1,
                "version": "",
                "input_list": [],
                "output_list": [],
                "prerequisite": [],
                "description": "The script extracts the glycosylation disease information from the human_protein_disease_glyco.csv that is compiled from human_glyco-phenotype_disease_curation_list_v12-18-74.csv. The script maps the UniProtKB accessions to the UniprotKB canonical accessions. "
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        ]
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        ],
        "script": [
            {
                "uri": {
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                    "filename": "make-protein-dataset.py"
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            }
        ]
    },
    "parametric_domain": [
        {
            "step": "",
            "param": "",
            "value": ""
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        "Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus on the gene-phenotype relationship. ",
        "The Monarch Initiative is focused primarily on phenotype-related resources and brings in data associated with those phenotypes so that the users can begin to make connections among other biological entities of interest. ",
        "If you are using this dataset please give proper attribution to OMIM, Monarch Initiative, EMBL-EBI-UniProt and GlyGen. "
    ],
    "etag": "306d5892bcae3a3718a48b70f4842c4c",
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            },
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}