Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_provenance.
- NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_assertion description "[Thus, the hypothesis that ?-thalassemia individuals, who are homozygous for the 118 kb deletion, may also have an exacerbation of their anemia due to the deletion of two copies of the ?-globin enhancer element is worthy of consideration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_provenance.
- NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_assertion evidence source_evidence_literature NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_provenance.
- NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_assertion SIO_000772 21390308 NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_provenance.
- NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_assertion wasDerivedFrom befree-20140225 NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_provenance.
- NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_assertion wasGeneratedBy ECO_0000203 NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP235730.RACCvkYyeP0bDO5KOlxm8GEGhfE4hAeoq38Ob1XZTFroc130_provenance.