Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_provenance.
- NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_assertion description "[In a study of G6PD deficient patients who presented with clinical favism in Spain, we have found a new polymorphic variant that we have called G6PD Malaga, whose only abnormality is a 542 A-->T (181 Asp-->Val) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_provenance.
- NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_assertion evidence source_evidence_literature NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_provenance.
- NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_assertion SIO_000772 8956035 NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_provenance.
- NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_assertion wasDerivedFrom befree-20140225 NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_provenance.
- NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_assertion wasGeneratedBy ECO_0000203 NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP672502.RAC9cmmW3pMk3oQP3DP1AzoaHQBSG-LajbVdFTyr8RlZY130_provenance.