Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_provenance.
- NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_assertion description "[To identify additional independently associated genetic variants, we performed a genome-wide association study (GWAS) on the proportion of F-cells in individuals of African ancestry with SCD from the Silent Infarct Transfusion (SIT) Trial cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_provenance.
- NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_assertion evidence source_evidence_literature NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_provenance.
- NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_assertion SIO_000772 21326311 NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_provenance.
- NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_assertion wasDerivedFrom befree-20140225 NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_provenance.
- NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_assertion wasGeneratedBy ECO_0000203 NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP416239.RARfJ3QSTsCIUpYdUaHhlSM_Y5VBnCvXILZaLtBDnILxk130_provenance.