Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_provenance.
- NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_assertion description "[This case is the third report of t(2;11) leukaemia with NUP98-HOXD13 and the first report showing that NUP98 rearrangements are associated with infant leukaemia, as well as therapy-related acute myelogenous leukaemia or myelodysplastic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_provenance.
- NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_assertion evidence source_evidence_literature NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_provenance.
- NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_assertion SIO_000772 10931000 NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_provenance.
- NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_assertion wasDerivedFrom befree-20140225 NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_provenance.
- NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_assertion wasGeneratedBy ECO_0000203 NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP635136.RATrhaG2LeMkAv5sAhDZTE9gjWJnrxibePCEPaQSip7tw130_provenance.