Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_provenance.
- NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_assertion description "[These findings suggest that genetic variations in TIMP1, TIMP3, MMP10, and ELN genes may contribute to the pathogenesis of AAAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_provenance.
- NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_assertion evidence source_evidence_literature NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_provenance.
- NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_assertion SIO_000772 15944607 NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_provenance.
- NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_assertion wasDerivedFrom gad-20130706 NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_provenance.
- NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_assertion wasGeneratedBy ECO_0000203 NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_provenance.
- gad-20130706 importedOn "2013-07-06" NP62602.RAWmfH_wNV887_UNg-OT5KsRTwRnpVAEWhmcOnSMCejQo130_provenance.