Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_provenance.
- NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_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." NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_provenance.
- NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_assertion evidence source_evidence_literature NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_provenance.
- NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_assertion SIO_000772 19074885 NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_provenance.
- NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_assertion wasDerivedFrom gad-20130706 NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_provenance.
- NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_assertion wasGeneratedBy ECO_0000203 NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_provenance.
- gad-20130706 importedOn "2013-07-06" NP81883.RAJYRBP_O0ws9NRRw5-t31TqLK5NKGlEXJ9x55-gvqh2o130_provenance.