Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_assertion> ?p ?o ?g. }
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- NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_assertion type Assertion NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_head.
- NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_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." NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_provenance.
- NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_assertion evidence source_evidence_literature NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_provenance.
- NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_assertion SIO_000772 12093744 NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_provenance.
- NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_assertion wasDerivedFrom befree-20140225 NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_provenance.
- NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_assertion wasGeneratedBy ECO_0000203 NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_provenance.