Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_provenance.
- NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_assertion description "[Remarkably, most of the genes showing distinctive expression in oligodendroglioma with 1p loss were also highly expressed in normal brain tissues and had neuron-related function, which included MYT1L, INA, RIMS2, SNAP97 and SNCB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_provenance.
- NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_assertion evidence source_evidence_literature NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_provenance.
- NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_assertion SIO_000772 14997935 NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_provenance.
- NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_assertion wasDerivedFrom befree-20140225 NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_provenance.
- NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_assertion wasGeneratedBy ECO_0000203 NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP532015.RArDMxmfhuz_pfixmJZPVCX_gQ-_XRxe2mcOgs8G_RAYs130_provenance.