Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_provenance.
- NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_assertion wasGeneratedBy ECO_0000203 NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_provenance.
- NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_assertion wasDerivedFrom befree-20140225 NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_provenance.
- NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_assertion SIO_000772 18667698 NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_provenance.
- NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_assertion evidence source_evidence_literature NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_provenance.
- NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_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." NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP335190.RAZ4wRh9861qYhKR_vPvFUHYmxp1sNRf5vXJSG7mY5cxc130_provenance.