Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_provenance.
- NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_assertion wasGeneratedBy ECO_0000203 NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_provenance.
- NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_assertion wasDerivedFrom befree-20150227 NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_provenance.
- NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_assertion SIO_000772 18667698 NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_provenance.
- NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_assertion evidence source_evidence_literature NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_provenance.
- NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_assertion description "[Here, we genotyped additional BCL11A SNPs, HBS1L-MYB SNPs, and an SNP upstream of (G)gamma-globin (HBG2; the XmnI polymorphism), in two independent SCD cohorts: the African American Cooperative Study of Sickle Cell Disease (CSSCD) and an SCD cohort from Brazil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444623.RAWz7rxYUvCWbTnUcTfHhFkfdoVd2c2yGP_gVtkf19q4c130_provenance.