Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_provenance.
- NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_assertion description "[Our case confirms that the inv(11) is a rare chromosomal translocation that is associated with therapy-related or de novo myeloid malignancy and involves NUP98 and DDX10 but not MLL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_provenance.
- NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_assertion evidence source_evidence_literature NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_provenance.
- NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_assertion SIO_000772 10222653 NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_provenance.
- NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_assertion wasDerivedFrom befree-20150227 NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_provenance.
- NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_assertion wasGeneratedBy ECO_0000203 NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP601110.RA1227gLHVawrU1WbvkR_n4ch9zhEidFMjziGkytPVrUI130_provenance.