Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_provenance.
- NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_assertion wasGeneratedBy ECO_0000203 NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_provenance.
- NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_assertion wasDerivedFrom gad-20150221 NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_provenance.
- NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_assertion SIO_000772 18667698 NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_provenance.
- NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_assertion evidence source_evidence_literature NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_provenance.
- NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_assertion description "[Together, common SNPs at the BCL11A, HBS1L-MYB, and beta-globin (HBB) loci account for >20% of the variation in HbF levels in SCD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP127468.RA_PiIIRGOoXHb9z86u87K58eWj2pr5c-ufbZi1dHyGTQ130_provenance.