Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_provenance.
- NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_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." NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_provenance.
- NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_assertion evidence source_evidence_literature NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_provenance.
- NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_assertion SIO_000772 15755899 NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_provenance.
- NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_assertion wasDerivedFrom befree-20140225 NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_provenance.
- NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_assertion wasGeneratedBy ECO_0000203 NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP361886.RAm6tkgynpx_er53IcC3e7DbSrUrG4LNbM_9whAPDLSuw130_provenance.