Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_provenance.
- NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_assertion description "[In addition, we found a significant interaction between the polymorphism and gender for MMP10 ( P = .037) in cases without a family history of AAA, as well as between the polymorphism and country of origin for ELN ( P = .0169) and TIMP3 ( P = .0023) in cases with a family history of AAA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_provenance.
- NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_assertion evidence source_evidence_literature NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_provenance.
- NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_assertion SIO_000772 15944607 NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_provenance.
- NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_assertion wasDerivedFrom befree-20140225 NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_provenance.
- NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_assertion wasGeneratedBy ECO_0000203 NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP270715.RAL2GeQHVnIjG0q3cZxBgaGDS6B4ciJXs90mxYyts-uOM130_provenance.