Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance.
- NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_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." NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance.
- NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_assertion evidence source_evidence_literature NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance.
- NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_assertion SIO_000772 12093744 NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance.
- NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_assertion wasDerivedFrom befree-20140225 NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance.
- NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_assertion wasGeneratedBy ECO_0000203 NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance.