Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_provenance.
- NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_assertion description "[These results provide genetic basis for gender differences in MDD and will serve as a resource for replication in other populations to elucidate the potential role of these genetic variants in MDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_provenance.
- NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_assertion evidence source_evidence_literature NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_provenance.
- NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_assertion SIO_000772 21621269 NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_provenance.
- NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_assertion wasDerivedFrom gad-20150221 NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_provenance.
- NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_assertion wasGeneratedBy ECO_0000203 NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP189792.RAUxdoChmZN9dGXaEGo-9nx2CekJ52E9NsgZzyk56rAXg130_provenance.