Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_provenance.
- NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_assertion description "[ZNF198, mapping to 13q11-q12, was recently shown to fuse to the fibroblast growth factor receptor 1 gene in the t(8;13)(p11;q11-q12) rearrangement associated with a stem cell leukemia/lymphoma syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_provenance.
- NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_assertion evidence source_evidence_literature NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_provenance.
- NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_assertion SIO_000772 10486218 NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_provenance.
- NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_assertion wasDerivedFrom befree-20140225 NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_provenance.
- NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_assertion wasGeneratedBy ECO_0000203 NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP921189.RAQNXPaP0y2-vcXG9vNJHiivRvRFIDJ3qVSVHHPEOHEkg130_provenance.