Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_provenance.
- NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_assertion description "[By analyzing several genes with very high ('spiked') expression in individual cases, we identified clusters with different biologic characteristics, such as samples with MALT1 translocations having high expression of MALT1 and RARA, samples with plasmacytic differentiation having high FKBP11 expression, and samples with high RGS13 expression tending to have trisomy 3 and reactive follicles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_provenance.
- NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_assertion evidence source_evidence_literature NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_provenance.
- NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_assertion SIO_000772 18974375 NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_provenance.
- NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_assertion wasDerivedFrom befree-20150227 NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_provenance.
- NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_assertion wasGeneratedBy ECO_0000203 NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP671791.RAgqnGBwxuBgMS_QPofJdCYyGSS6b9vA_ADQHJRPnQYxg130_provenance.