Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_provenance.
- NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_assertion description "[Using a NUP98-HOXD13 fusion gene, we have developed a mouse model that faithfully recapitulates all of the key features of MDS, including peripheral blood cytopenias, bone marrow dysplasia, and apoptosis, and transformation to acute leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_provenance.
- NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_assertion evidence source_evidence_literature NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_provenance.
- NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_assertion SIO_000772 15755899 NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_provenance.
- NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_assertion wasDerivedFrom befree-20150227 NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_provenance.
- NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_assertion wasGeneratedBy ECO_0000203 NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914103.RA39YMV_AtacMwA6jwndSuKFEcYg3eQTbOZXXvEmkkN_Q130_provenance.