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- NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_assertion type Assertion NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_head.
- NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_provenance.
- NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_assertion evidence source_evidence_literature NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_provenance.
- NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_assertion SIO_000772 12093744 NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_provenance.
- NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_assertion wasDerivedFrom befree-20140225 NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_provenance.
- NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_assertion wasGeneratedBy ECO_0000203 NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_provenance.