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"accession": "CLO:0024576",
"name": "GM05610 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
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"accession": "CLO:0024569",
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"definition": "[' HUNTINGTON DISEASE; HD']",
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"definition": "[' HUNTINGTON DISEASE; HD']",
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{
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"definition": "[' HUNTINGTON DISEASE; HD']",
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{
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"name": "GM05600 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
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{
"accession": "CLO:0024565",
"name": "GM05594 cell",
"definition": "[' HUNTINGTON DISEASE; HD APPARENTLY HEALTHY NON-FETAL TISSUE']",
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},
{
"accession": "CLO:0024566",
"name": "GM05590 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
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{
"accession": "CLO:0024558",
"name": "GM05584 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
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{
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"name": "GM05580 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
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{
"accession": "CLO:0024556",
"name": "GM05572 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
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{
"accession": "CLO:0024549",
"name": "GM05569 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA']",
"term_type": "cell line"
},
{
"accession": "CLO:0024551",
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"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
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{
"accession": "CLO:0024545",
"name": "GM05564 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0024547",
"name": "GM05563 cell",
"definition": "[' RING CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0024775",
"name": "GM05560 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
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"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
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{
"accession": "CLO:0024785",
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"definition": "[' HUNTINGTON DISEASE; HD']",
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}
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}