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{
"accession": "CLO:0002972",
"name": "F2 cell",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "CLO:0002977",
"name": "F32 VIII C4 cell",
"definition": "['disease: hybridoma']",
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{
"accession": "CLO:0002978",
"name": "F3B6 cell",
"definition": "['disease: hybridoma fusion partner']",
"term_type": "cell line"
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{
"accession": "CLO:0002979",
"name": "F4/4.K6 cell",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "CLO:0002981",
"name": "F45J cell",
"definition": "['disease: hybridoma']",
"term_type": "cell line"
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{
"accession": "CLO:0002980",
"name": "F4/80 cell",
"definition": "['disease: hybridoma']",
"term_type": "cell line"
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{
"accession": "CLO:0002982",
"name": "F4N (MEL) cell",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "CLO:0002984",
"name": "F5-A-1/22.8.13 cell",
"definition": "['disease: hybridoma']",
"term_type": "cell line"
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{
"accession": "CLO:0002983",
"name": "F5 cell",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "CLO:0002985",
"name": "F7000 cell",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "CLO:0002987",
"name": "F89 cell",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "CLO:0002986",
"name": "F8 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0002989",
"name": "F94 cell",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "CLO:0002990",
"name": "F95 cell",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "CLO:0002991",
"name": "F96 cell",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "CLO:0002992",
"name": "F98 cell",
"definition": "['disease: undifferentiated malignant glioma']",
"term_type": "cell line"
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{
"accession": "CLO:0002988",
"name": "F9 cell",
"definition": "['disease: embryonic carcinoma; testicular teratoma']",
"term_type": "cell line"
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{
"accession": "CLO:0037255",
"name": "FA2N-4 cell",
"definition": "['FA2N-4 is a human hepatocyte cell line. Reference: http://web.expasy.org/cellosaurus/CVCL_0267']",
"term_type": "cell line"
},
{
"accession": "DOID:14499",
"name": "Fabry disease",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "UBERON:0001456",
"name": "face",
"definition": "['A subdivision of the head that has as parts the layers deep to the surface of the anterior surface, including the mouth, eyes, and nose (when present). In vertebrates, this includes the facial skeleton and structures superficial to the facial skeleton (cheeks, mouth, eyeballs, skin of face, etc).']",
"term_type": "cell line"
}
]
}