Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_provenance.
- NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_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." NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_provenance.
- NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_assertion evidence source_evidence_literature NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_provenance.
- NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_assertion SIO_000772 19074885 NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_provenance.
- NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_assertion wasDerivedFrom befree-20140225 NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_provenance.
- NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_assertion wasGeneratedBy ECO_0000203 NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP833059.RAt2ffGWwJ7d2QOc79841fEGJnWRFeK6HZ1HuM1BCEiBk130_provenance.