Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_provenance.
- befree-2016 importedOn "2016-02-19" NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_provenance.
- NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_assertion wasGeneratedBy ECO_0000203 NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_provenance.
- NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_assertion wasDerivedFrom befree-2016 NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_provenance.
- NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_assertion SIO_000772 11782354 NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_provenance.
- NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_assertion evidence source_evidence_literature NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_provenance.
- NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_assertion description "[Our results revealed that t(2;11)(q31;p15) was not a single chromosomal abnormality and that the NUP98-HOXD fusion genes encode similar fusion proteins, which suggests that the NUP98-HOXD11 as well as NUP98-HOXD13 fusion protein play a role in leukemogenesis through similar mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP341521.RAe_U2iUg8fBkAneaT53E-4KfGBRE1QAcVfJ56FKbuwio130_provenance.