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- source_evidence_literature type ECO_0000212 NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_provenance.
- NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_assertion wasGeneratedBy ECO_0000203 NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_provenance.
- NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_assertion wasDerivedFrom befree-20150227 NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_provenance.
- NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_assertion SIO_000772 17021403 NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_provenance.
- NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_assertion evidence source_evidence_literature NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_provenance.
- NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_assertion description "[Identification of der(1;19)(q10;p10) in five oligodendrogliomas suggests mechanism of concurrent 1p and 19q loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP942615.RAaqFXkIaf4haAWdnhby3DnTrcGfeGu7zq_rutelRwiRw130_provenance.