Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_provenance.
- NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_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." NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_provenance.
- NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_assertion evidence source_evidence_literature NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_provenance.
- NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_assertion SIO_000772 10583265 NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_provenance.
- NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_assertion wasDerivedFrom befree-20140225 NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_provenance.
- NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_assertion wasGeneratedBy ECO_0000203 NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP771021.RAub4l2hmPhe2HjLkaCQ2fQ8NsOkhRVjcJ0S21PYmPKOY130_provenance.