Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_provenance.
- NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_assertion description "[Our findings confirm that additional or secondary genetic changes including AML1 amplification are commonly encountered in childhood ALL with TEL/AML1 gene fusion, which are envisaged to play significant roles in disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_provenance.
- NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_assertion evidence source_evidence_literature NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_provenance.
- NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_assertion SIO_000772 11516105 NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_provenance.
- NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_assertion wasDerivedFrom befree-2016 NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_provenance.
- NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_assertion wasGeneratedBy ECO_0000203 NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_provenance.
- befree-2016 importedOn "2016-02-19" NP327751.RAer012ZD3zg8ESUWLA8ljlaz0w81HovVlTrwmoaTQRcw130_provenance.