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{
"accession": "MS:1002297",
"name": "EVOQ Elite",
"definition": "Bruker Daltonics' EVOQ Elite: LC-triple quadrupole.",
"term_type": "instrument"
},
{
"accession": "MS:1002298",
"name": "EVOQ Qube",
"definition": "Bruker Daltonics' EVOQ Qube: LC-triple quadrupole.",
"term_type": "instrument"
},
{
"accession": "NCBITaxon:2605435",
"name": "Evosea",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0002955",
"name": "EVSA-T cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0009867",
"name": "EW-11 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0009868",
"name": "EW-13 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0009869",
"name": "EW-16 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0009870",
"name": "EW-18 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0009866",
"name": "EW-1 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0009871",
"name": "EW-24 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0009872",
"name": "EW-3 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0009873",
"name": "EW-7 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:3369",
"name": "Ewing sarcoma",
"definition": "['A connective tissue cancer that has_material_basis in neural crest cells derives_from undeveloped, undifferentiated neuroectoderm.', 'OMIM mapping confirmed by DO. [SN].']",
"term_type": "cell line"
},
{
"accession": "DOID:3368",
"name": "Ewing sarcoma of bone",
"definition": "['A peripheral primitive neuroectodermal tumor that is located_in bone.']",
"term_type": "cell line"
},
{
"accession": "EFO:0000174",
"name": "Ewings sarcoma",
"definition": "['A malignant tumor of the bone which always arises in the medullary tissue, occurring more often in cylindrical bones. There are conspicuous foci of necrosis in association with irregular masses of small, regular, rounded or ovoid cells with very scanty cytoplasm. The tumor occurs usually before the age of 20, about twice as frequently in males as in females. (From Dorland, 27th ed; Stedman, 25th ed)', \"A small round cell tumor that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing's sarcoma/peripheral neuroectodermal tumor. It affects mostly males under age 20, and it can occur in soft tissue or bone. Pain and the presence of a mass are the most common clinical symptoms.\", 'A spectrum of malignant tumors, affecting mostly males under age 20, characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of a spectrum, with Ewing sarcoma lacking evidence of neural differentiation and the markers that characterize the peripheral primitive neuroectodermal tumor. Ewing sarcoma and peripheral primitive neuroectodermal tumor may share cytogenetic abnormalities, proto-oncogene expression, cell culture and immunohistochemical abnormalities. These tumors may occur in the soft tissues or the bones. Pain and the presence of a mass are the most common clinical symptoms.', 'A spectrum of malignant tumors, affecting mostly males under age 20, characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of a spectrum, with Ewing sarcoma lacking evidence of neural differentiation and the markers that characterize the peripheral primitive neuroectodermal tumor. Ewing sarcoma and peripheral primitive neuroectodermal tumor may share cytogenetic abnormalities, proto-oncogene expression, cell culture and immunohistochemical abnormalities. These tumors may occur in the soft tissues or the bones. Pain and the presence of a mass are the most common clinical symptoms. -- 2004\\n']",
"term_type": "cell line"
},
{
"accession": "DOID:4158",
"name": "Ewings sarcoma-primitive neuroectodermal tumor (PNET)",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "MS:1000649",
"name": "Exactive",
"definition": "Thermo Scientific Exactive MS.",
"term_type": "instrument"
},
{
"accession": "MS:1002526",
"name": "Exactive Plus",
"definition": "Thermo Scientific Exactive Plus MS.",
"term_type": "instrument"
},
{
"accession": "GO:0098976",
"name": "excitatory chemical synaptic transmission",
"definition": "['Synaptic transmission that results in an excitatory postsynaptic potential.']",
"term_type": "cell line"
},
{
"accession": "CL:0008030",
"name": "excitatory neuron",
"definition": "[]",
"term_type": "cell line"
}
]
}