Mercurial > repos > iuc > beacon2_csv2xlsx

comparison test-data/EGAF00005572902.json @ 0:4509627e6ee1 draft default tip

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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/beacon2 commit dcaf8046840f163143075b276dd75909d344ec3a
author iuc
date Sun, 01 Oct 2023 16:29:22 +0000
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-1:000000000000 0:4509627e6ee1
1 {
2 "phenopacket": {
3 "id": "P0244875",
4 "subject": {
5 "id": "P0244875",
6 "dateOfBirth": "1987-01-01T00:00:00Z",
7 "sex": "MALE"
8 },
9 "phenotypicFeatures": [],
10 "diseases": [],
11 "genes": [],
12 "variants": [],
13 "meta_data": {
14 "created": "2021-04-21T09:51:14.643Z",
15 "resources": [
16 {
17 "id": "hp",
18 "name": "Human Phenotype Ontology",
19 "url": "http://purl.obolibrary.org/obo/hp.owl",
20 "version": "2020-12-07",
21 "namespacePrefix": "HP",
22 "iriPrefix": "http://purl.obolibrary.org/obo/HP_"
23 },
24 {
25 "id": "orphanet",
26 "name": "Orphanet Rare Disease Ontology",
27 "url": "http://orpha.net/ontology/ORDO_en_3.1.owl",
28 "version": "3.1",
29 "namespacePrefix": "Orphanet",
30 "iriPrefix": "http://www.orpha.net/ORDO/Orphanet_"
31 },
32 {
33 "id": "hgnc",
34 "name": "HUGO Gene Nomenclature Committee",
35 "url": "https://www.genenames.org",
36 "version": "2021-01-13",
37 "namespacePrefix": "HGNC",
38 "iriPrefix": "https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/"
39 },
40 {
41 "id": "mim",
42 "name": "Online Mendelian Inheritance in Man",
43 "url": "https://omim.org/",
44 "version": "2021-01-21",
45 "namespacePrefix": "OMIM",
46 "iriPrefix": "https://omim.org/entry/"
47 }
48 ]
49 }
50 },
51 "interpretation": {
52 "id": "P0244875",
53 "resolutionStatus": "UNKNOWN",
54 "phenopacket": {
55 "id": "P0244875",
56 "subject": {
57 "id": "P0244875",
58 "dateOfBirth": "1987-01-01T00:00:00Z",
59 "sex": "MALE"
60 },
61 "phenotypicFeatures": [],
62 "diseases": [],
63 "genes": [],
64 "variants": [],
65 "meta_data": {
66 "created": "2021-04-21T09:51:14.643Z",
67 "resources": [
68 {
69 "id": "hp",
70 "name": "Human Phenotype Ontology",
71 "url": "http://purl.obolibrary.org/obo/hp.owl",
72 "version": "2020-12-07",
73 "namespacePrefix": "HP",
74 "iriPrefix": "http://purl.obolibrary.org/obo/HP_"
75 },
76 {
77 "id": "orphanet",
78 "name": "Orphanet Rare Disease Ontology",
79 "url": "http://orpha.net/ontology/ORDO_en_3.1.owl",
80 "version": "3.1",
81 "namespacePrefix": "Orphanet",
82 "iriPrefix": "http://www.orpha.net/ORDO/Orphanet_"
83 },
84 {
85 "id": "hgnc",
86 "name": "HUGO Gene Nomenclature Committee",
87 "url": "https://www.genenames.org",
88 "version": "2021-01-13",
89 "namespacePrefix": "HGNC",
90 "iriPrefix": "https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/"
91 },
92 {
93 "id": "mim",
94 "name": "Online Mendelian Inheritance in Man",
95 "url": "https://omim.org/",
96 "version": "2021-01-21",
97 "namespacePrefix": "OMIM",
98 "iriPrefix": "https://omim.org/entry/"
99 }
100 ]
101 }
102 },
103 "diagnosis": [],
104 "meta_data": {}
105 }
106 }