Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_provenance.
- NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_assertion description "[NUP98/NSD1-positive AML cases had significantly higher white blood cell counts (median, 147 � 10?/L), more frequent FAB-M4/M5 morphology (in 63%), and more CN-AML (in 78%), FLT3/internal tandem duplication (in 91%) and WT1 mutations (in 45%) than NUP98/NSD1-negative cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_provenance.
- NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_assertion evidence source_evidence_literature NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_provenance.
- NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_assertion SIO_000772 21813447 NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_provenance.
- NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_assertion wasDerivedFrom befree-2016 NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_provenance.
- NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_assertion wasGeneratedBy ECO_0000203 NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_provenance.
- befree-2016 importedOn "2016-02-19" NP914484.RAxupBzUm5Z2fVLsdZCZ72npdm86sENu3SmZcLkOss3dw130_provenance.