Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_provenance.
- NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_assertion description "[The chromosomal translocation t(7; 11)(p15;p15), observed in human myeloid leukemia, results in a NUP98 and HOXA9 gene fusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_provenance.
- NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_assertion evidence source_evidence_literature NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_provenance.
- NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_assertion SIO_000772 15454493 NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_provenance.
- NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_assertion wasDerivedFrom befree-20140225 NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_provenance.
- NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_assertion wasGeneratedBy ECO_0000203 NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP679435.RAyYttL-aMb65oLsTXMlRGMzY4A1fgOTF2JFNiuufbVfU130_provenance.