Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_provenance.
- NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_assertion description "[Somatic, heterozygous ASXL1 mutations were identified in 14/48 (29%) of patients with GATA2 deficiency, including four out of five patients who developed a proliferative chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_provenance.
- NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_assertion evidence source_evidence_literature NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_provenance.
- NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_assertion SIO_000772 24077845 NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_provenance.
- NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_assertion wasDerivedFrom befree-20150227 NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_provenance.
- NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_assertion wasGeneratedBy ECO_0000203 NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP418967.RAEXEYURROgCnywJDc2LMEJp4UQfRdDZiLQqx3F18K3cg130_provenance.