Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_provenance.
- NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_assertion description "[We performed whole transcriptome sequencing to identify fusion genes in glioma and discovered FGFR3-TACC3 fusions in 4 of 48 glioblastoma samples from patients both of mixed European and of Asian descent, but not in any of 43 low-grade glioma samples tested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_provenance.
- NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_assertion evidence source_evidence_literature NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_provenance.
- NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_assertion SIO_000772 23298836 NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_provenance.
- NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_assertion wasDerivedFrom befree-20140225 NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_provenance.
- NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_assertion wasGeneratedBy ECO_0000203 NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP723848.RACZYscqEN96h3Eob10Dtz305YzW0PmHvAqoKTNL4-aBM130_provenance.