Mercurial > repos > iuc > beacon2_pxf2bff
view test-data/individuals.json @ 1:23449c685168 draft default tip
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/beacon2 commit eecd43b81a8c9f2175c50a71ae85ce9185a9d3a7
author | iuc |
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date | Tue, 16 Apr 2024 09:27:25 +0000 |
parents | 30605b5fc43f |
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Man", "namespacePrefix" : "OMIM", "url" : "https://omim.org/", "version" : "2021-01-21" } ] }, "variants" : [] } }, "phenotypicFeatures" : [], "sex" : { "id" : "NCIT:C20197", "label" : "male" } }, { "diseases" : [], "id" : "P0007503", "info" : { "interpretation" : { "diagnosis" : [], "phenopacket" : { "meta_data" : { "created" : "2021-04-21T09:39:45.571Z", "resources" : [ { "id" : "hp", "iriPrefix" : "http://purl.obolibrary.org/obo/HP_", "name" : "Human Phenotype Ontology", "namespacePrefix" : "HP", "url" : "http://purl.obolibrary.org/obo/hp.owl", "version" : "2020-12-07" }, { "id" : "orphanet", "iriPrefix" : "http://www.orpha.net/ORDO/Orphanet_", "name" : "Orphanet Rare Disease Ontology", "namespacePrefix" : "Orphanet", "url" : "http://orpha.net/ontology/ORDO_en_3.1.owl", "version" : "3.1" }, { "id" : "hgnc", "iriPrefix" : "https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/", "name" : "HUGO Gene Nomenclature Committee", "namespacePrefix" : "HGNC", "url" : 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