Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance.
- NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_assertion description "[The study revealed that 4 genotypes (- -(SEA)/ -alpha(3.7), - -(SA)/-alpha(3.7), - -(SEA)/-alpha(3.7 Sallanches), - -alpha(3.7)/-alpha(3.7 Sallanches)) were responsible for Hb H disease, the alpha+ thalassemia mutation (-alpha(3.7) deletion) being the most common defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance.
- NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_assertion evidence source_evidence_literature NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance.
- NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_assertion SIO_000772 20154289 NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance.
- NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_assertion wasDerivedFrom befree-20140225 NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance.
- NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_assertion wasGeneratedBy ECO_0000203 NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance.