Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance.
- NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_assertion description "[Erythrocyte ghosts from eight individuals with hereditary spherocytosis have been compared with respect to their protein compositions as judged by SDS gel electrophoresis, their ease of spectrin extractability, and their freeze-etch electron microscopic appearance after incubation in condition designed to promote aggregation of the intramembrane particles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance.
- NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_assertion evidence source_evidence_literature NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance.
- NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_assertion SIO_000772 6849841 NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance.
- NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_assertion wasDerivedFrom befree-20140225 NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance.
- NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_assertion wasGeneratedBy ECO_0000203 NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance.