Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_provenance.
- NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_assertion description "[We hypothesized that functional polymorphisms in GSTT1 (gene deletion) and CYP1A1 (m1, m2, and m3) might be associated with SIDS risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_provenance.
- NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_assertion evidence source_evidence_literature NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_provenance.
- NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_assertion SIO_000772 16763966 NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_provenance.
- NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_assertion wasDerivedFrom gad-20130706 NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_provenance.
- NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_assertion wasGeneratedBy ECO_0000203 NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP87447.RAecpp4xc75fY88ZzMU-QN2JeTbu7JWTrRFEqeg0Z4kLE130_provenance.