Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_provenance.
- NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_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." NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_provenance.
- NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_assertion evidence source_evidence_literature NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_provenance.
- NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_assertion SIO_000772 19074885 NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_provenance.
- NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_assertion wasDerivedFrom gad-20150221 NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_provenance.
- NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_assertion wasGeneratedBy ECO_0000203 NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP101546.RA7naRuQlxf_R0eVUvQYXJSLkSu_3i7vZeOE5bws_HinM130_provenance.