Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_assertion> ?p ?o ?g. }
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- NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_assertion type Assertion NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_head.
- NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_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." NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_provenance.
- NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_assertion evidence source_evidence_literature NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_provenance.
- NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_assertion SIO_000772 12093744 NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_provenance.
- NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_assertion wasDerivedFrom befree-20150227 NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_provenance.
- NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_assertion wasGeneratedBy ECO_0000203 NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_provenance.