Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_provenance.
- NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_assertion description "[Molecular heterogeneity of the NUP98/HOXA9 fusion transcript in myelodysplastic syndromes associated with t(7;11)(p15;p15).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_provenance.
- NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_assertion evidence source_evidence_literature NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_provenance.
- NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_assertion SIO_000772 10583265 NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_provenance.
- NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_assertion wasDerivedFrom befree-20140225 NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_provenance.
- NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_assertion wasGeneratedBy ECO_0000203 NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP675505.RAzeZQDO4Vlb-X637FgpEJnp21iKAcTvktO7UdLjPadPU130_provenance.