Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_provenance.
- NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_assertion description "[Disruption of HRX as a result of chromosomal translocation is thought to contribute to the leukaemogenic process; this may occur in utero giving rise to infant acute leukaemia or may be induced by epipodophyllotoxic drugs resulting in secondary leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_provenance.
- NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_assertion evidence source_evidence_literature NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_provenance.
- NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_assertion SIO_000772 7920216 NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_provenance.
- NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_assertion wasDerivedFrom befree-20150227 NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_provenance.
- NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_assertion wasGeneratedBy ECO_0000203 NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP787067.RAATQAYityxkGdFuWzZSKemw2k3Uxlrb5RPSpWVhhFGoo130_provenance.