Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_provenance.
- NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_assertion wasGeneratedBy ECO_0000203 NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_provenance.
- NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_assertion wasDerivedFrom befree-20140225 NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_provenance.
- NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_assertion SIO_000772 23161389 NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_provenance.
- NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_assertion evidence source_evidence_literature NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_provenance.
- NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_assertion description "[Typical HPFH is associated with promoter mutations or large deletions affecting the human fetal globin (HBG1 and HBG2) genes, while genetic defects in other genes involved in human erythropoiesis, e.g.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP586374.RABpRxpPkdD_cWjBj_I9tgNgBwPqZA6A9F2EgC5N37XS4130_provenance.