Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_provenance.
- NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_assertion description "[Homozygous CYP1A1*2A genotype was underrepresented in ALL patients (1%) as compared to control (4.8%) but the differences did not reach to statistical significance (OR 0.21; 95% CI 0.03-1.72).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_provenance.
- NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_assertion evidence source_evidence_literature NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_provenance.
- NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_assertion SIO_000772 12827651 NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_provenance.
- NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_assertion wasDerivedFrom gad-20150221 NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_provenance.
- NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_assertion wasGeneratedBy ECO_0000203 NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_provenance.
- gad-20150221 importedOn "2015-02-21" NP80395.RAlfI-FWDbXqs5yH_rcLcXPmamCOhiTWOtQfdwJ51TK_Y130_provenance.