Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_provenance.
- NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_assertion description "[NUP98 is fused to PMX1 homeobox gene in human acute myelogenous leukemia with chromosome translocation t(1;11)(q23;p15).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_provenance.
- NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_assertion evidence source_evidence_literature NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_provenance.
- NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_assertion SIO_000772 10397741 NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_provenance.
- NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_assertion wasDerivedFrom befree-20150227 NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_provenance.
- NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_assertion wasGeneratedBy ECO_0000203 NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP632893.RANY2ep2K1e7TsyI5543CtScQXNp3-ZDtRov9M46yUSQM130_provenance.