Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_provenance.
- NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_assertion description "[We evaluated the association between genetic polymorphisms (SNPs) in 12 JAK/STAT pathway genes (JAK3, STAT1, STAT2, STAT3, STAT4, STAT5a, STAT5b, STAT6, SCOS1, SCOS2, SCOS3, and SCOS4) and NHL risk in a population-based case-control study of Connecticut women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_provenance.
- NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_assertion evidence source_evidence_literature NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_provenance.
- NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_assertion SIO_000772 23768868 NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_provenance.
- NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_assertion wasDerivedFrom befree-20140225 NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_provenance.
- NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_assertion wasGeneratedBy ECO_0000203 NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP928029.RA_BbwpV-zb5lAGgRdSZDT7V5oiqC1rNXSB4T24n5wnGA130_provenance.