Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_provenance.
- NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_assertion description "[Gria4 deficient mice provide a model of AE, one for which the common laboratory inbred strain C3H/HeJ (HeJ) harbors a natural IAP retrotransposon insertion in Gria4 that reduces its expression 8-fold.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_provenance.
- NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_assertion evidence source_evidence_literature NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_provenance.
- NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_assertion SIO_000772 25010494 NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_provenance.
- NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_assertion wasDerivedFrom befree-20150227 NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_provenance.
- NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_assertion wasGeneratedBy ECO_0000203 NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP472708.RAYUFTFqxwR0XastW4Gp7zJhkLB6hK__6M-XFEBTv--ZQ130_provenance.