Source:http://linkedlifedata.com/resource/lhgdn/association:981
Predicate | Object |
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lhgdn:found_in | |
lhgdn:geneRifSource |
SOCS-1 hypermethylation was seen in patients with an autoactivating JAK2 mutation & those with wild-type JAK2/SOCS-1 inactivation may be a complementary mechanism to the JAK2V617F mutation in the pathogenesis of myeloproliferative disorders.
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lhgdn:mesh_code |
D009196
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lhgdn:associationIdType | |
lhgdn:umls_code |