Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance.
- NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_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." NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance.
- NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_assertion evidence source_evidence_literature NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance.
- NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_assertion SIO_000772 6935689 NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance.
- NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_assertion wasDerivedFrom befree-20140225 NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance.
- NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_assertion wasGeneratedBy ECO_0000203 NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance.