Mercurial > repos > iuc > beacon2_csv2xlsx

comparison test-data/EGAF00005572890.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": "P0008910",
4 "subject": {
5 "id": "P0008910",
6 "dateOfBirth": "unknown-01-01T00:00:00Z",
7 "sex": "FEMALE"
8 },
9 "phenotypicFeatures": [
10 {
11 "type": {
12 "id": "HP:0100615",
13 "label": "Ovarian neoplasm"
14 }
15 }
16 ],
17 "diseases": [],
18 "genes": [],
19 "variants": [],
20 "meta_data": {
21 "created": "2021-04-21T09:48:57.456Z",
22 "resources": [
23 {
24 "id": "hp",
25 "name": "Human Phenotype Ontology",
26 "url": "http://purl.obolibrary.org/obo/hp.owl",
27 "version": "2020-12-07",
28 "namespacePrefix": "HP",
29 "iriPrefix": "http://purl.obolibrary.org/obo/HP_"
30 },
31 {
32 "id": "orphanet",
33 "name": "Orphanet Rare Disease Ontology",
34 "url": "http://orpha.net/ontology/ORDO_en_3.1.owl",
35 "version": "3.1",
36 "namespacePrefix": "Orphanet",
37 "iriPrefix": "http://www.orpha.net/ORDO/Orphanet_"
38 },
39 {
40 "id": "hgnc",
41 "name": "HUGO Gene Nomenclature Committee",
42 "url": "https://www.genenames.org",
43 "version": "2021-01-13",
44 "namespacePrefix": "HGNC",
45 "iriPrefix": "https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/"
46 },
47 {
48 "id": "mim",
49 "name": "Online Mendelian Inheritance in Man",
50 "url": "https://omim.org/",
51 "version": "2021-01-21",
52 "namespacePrefix": "OMIM",
53 "iriPrefix": "https://omim.org/entry/"
54 }
55 ]
56 }
57 },
58 "interpretation": {
59 "id": "P0008910",
60 "resolutionStatus": "UNSOLVED",
61 "phenopacket": {
62 "id": "P0008910",
63 "subject": {
64 "id": "P0008910",
65 "dateOfBirth": "unknown-01-01T00:00:00Z",
66 "sex": "FEMALE"
67 },
68 "phenotypicFeatures": [
69 {
70 "type": {
71 "id": "HP:0100615",
72 "label": "Ovarian neoplasm"
73 }
74 }
75 ],
76 "diseases": [],
77 "genes": [],
78 "variants": [],
79 "meta_data": {
80 "created": "2021-04-21T09:48:57.456Z",
81 "resources": [
82 {
83 "id": "hp",
84 "name": "Human Phenotype Ontology",
85 "url": "http://purl.obolibrary.org/obo/hp.owl",
86 "version": "2020-12-07",
87 "namespacePrefix": "HP",
88 "iriPrefix": "http://purl.obolibrary.org/obo/HP_"
89 },
90 {
91 "id": "orphanet",
92 "name": "Orphanet Rare Disease Ontology",
93 "url": "http://orpha.net/ontology/ORDO_en_3.1.owl",
94 "version": "3.1",
95 "namespacePrefix": "Orphanet",
96 "iriPrefix": "http://www.orpha.net/ORDO/Orphanet_"
97 },
98 {
99 "id": "hgnc",
100 "name": "HUGO Gene Nomenclature Committee",
101 "url": "https://www.genenames.org",
102 "version": "2021-01-13",
103 "namespacePrefix": "HGNC",
104 "iriPrefix": "https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/"
105 },
106 {
107 "id": "mim",
108 "name": "Online Mendelian Inheritance in Man",
109 "url": "https://omim.org/",
110 "version": "2021-01-21",
111 "namespacePrefix": "OMIM",
112 "iriPrefix": "https://omim.org/entry/"
113 }
114 ]
115 }
116 },
117 "diagnosis": [],
118 "meta_data": {}
119 }
120 }