Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_provenance.
- NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_assertion description "[Further FISH indicated a breakpoint within fibroblast growth factor receptor 1 (FGFR1), the receptor tyrosine kinase that is known to be disrupted in a distinctive myeloproliferative disorder, most commonly by fusion to ZNF198.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_provenance.
- NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_assertion evidence source_evidence_literature NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_provenance.
- NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_assertion SIO_000772 11739186 NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_provenance.
- NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_assertion wasDerivedFrom befree-20140225 NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_provenance.
- NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_assertion wasGeneratedBy ECO_0000203 NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP568707.RAHFrbqTYKQ-p5v37BRVCqD4b3vHI7uAFQHDq5ZAyCS2M130_provenance.