Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_assertion> ?p ?o ?g. }
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- NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_assertion type Assertion NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_head.
- NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_assertion description "[Generation of the NUP98-HOXD13 fusion transcript by a rare translocation, t(2;11)(q31;p15), in a case of infant leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_provenance.
- NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_assertion evidence source_evidence_literature NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_provenance.
- NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_assertion SIO_000772 10931000 NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_provenance.
- NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_assertion wasDerivedFrom befree-20140225 NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_provenance.
- NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_assertion wasGeneratedBy ECO_0000203 NP485887.RAcecfMP11FnqRHsK-czGM3KWc4OyQBTnpvQESpfBkOzw130_provenance.