Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_provenance.
- NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_assertion description "[Novel NUP98-HOXC11 fusion gene resulted from a chromosomal break within exon 1 of HOXC11 in acute myeloid leukemia with t(11;12)(p15;q13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_provenance.
- NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_assertion evidence source_evidence_literature NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_provenance.
- NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_assertion SIO_000772 12183408 NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_provenance.
- NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_assertion wasDerivedFrom befree-20140225 NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_provenance.
- NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_assertion wasGeneratedBy ECO_0000203 NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP163591.RAeRCJtb93LWyPmbffWirym0O_wbYjEiYhIgfHK7J9DIc130_provenance.