Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_provenance.
- NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_assertion description "[We found association with CLL susceptibility and 22 haplotypes in APAF1, IL6, TNFRSF13B, IL16, CASP3, CCR7, LTA/TNF, BAX, BCL2, CXCL12, CASP10/CASP8, CASP1, CCL2, BAK1, and IL1A candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_provenance.
- NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_assertion evidence source_evidence_literature NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_provenance.
- NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_assertion SIO_000772 19074885 NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_provenance.
- NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_assertion wasDerivedFrom gad-20130706 NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_provenance.
- NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_assertion wasGeneratedBy ECO_0000203 NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_provenance.
- gad-20130706 importedOn "2013-07-06" NP82246.RAnzeb5jSz0ZKqlBa8PbPgJJLZDrWILk5DHM-cc_0Rfg8130_provenance.