Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance.
- NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_assertion description "[Whereas individuals heterozygous for most alpha-chain mutations possess approximately 25% abnormal hemoglobin, heterozygotes for the alpha-chain variant Hb G Philadelphia synthesize either 33% or 50% Hb G. Both variable gene dosage and interaction with alpha-thalassemia have been proposed to explain this observation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance.
- NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_assertion evidence source_evidence_literature NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance.
- NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_assertion SIO_000772 6935689 NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance.
- NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_assertion wasDerivedFrom befree-2016 NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance.
- NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_assertion wasGeneratedBy ECO_0000203 NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance.