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- source_evidence_literature type ECO_0000212 NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_provenance.
- NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_assertion description "[We found a significant association with an increased risk of AAA for MMP3 (AAA patients n = 1258, controls n = 1406: OR = 1.48 [95% CI = 1.23-1.78], I(2) = 0%) and MMP-13 (AAA patients n = 800, controls n = 843: OR = 1.37 [95% CI = 1.04-1.82], I(2) = 25%) polymorphisms and a trend that did not reach the statistical significance, toward a decreased risk of AAA for MMP2 (AAA patients n = 1090, controls n = 1077: OR = 0.83 [95% CI = .60-1.15], I(2) =7 1%) and ELN (AAA patients n = 904, controls n = 1069: OR = 0.79 [95% CI = .53-1.18], I(2) = 72%) polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_provenance.
- NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_assertion evidence source_evidence_literature NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_provenance.
- NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_assertion SIO_000772 22094117 NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_provenance.
- NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_assertion wasDerivedFrom befree-20150227 NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_provenance.
- NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_assertion wasGeneratedBy ECO_0000203 NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP561220.RAq3EBbkZW4VWEFqNe05uJDe1syHClPc2vQ8o371l79eA130_provenance.