Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_provenance.
- NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_assertion description "[To describe the hematological and molecular features as well as diagnostic aspects of a complex hemoglobinopathy caused by interaction of a novel ?2-globin chain variant with hemoglobin (Hb) E and ?(+)-thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_provenance.
- NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_assertion evidence source_evidence_literature NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_provenance.
- NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_assertion SIO_000772 21447006 NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_provenance.
- NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_assertion wasDerivedFrom befree-20140225 NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_provenance.
- NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_assertion wasGeneratedBy ECO_0000203 NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP589903.RAARUP0nsaoCcLHTHt0V6DYq1jl4NDD9lqz5oADq5QbYo130_provenance.