Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_assertion> ?p ?o ?g. }
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- NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_assertion type Assertion NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_head.
- NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_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." NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_provenance.
- NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_assertion evidence source_evidence_literature NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_provenance.
- NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_assertion SIO_000772 12093744 NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_provenance.
- NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_assertion wasDerivedFrom befree-20140225 NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_provenance.
- NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_assertion wasGeneratedBy ECO_0000203 NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_provenance.