Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_provenance.
- NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_assertion description "[In addition, seven other B-precursor ALL cases not bearing t(9;22) or t(11q23)/MLL chromosomal aberrations were analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_provenance.
- NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_assertion evidence source_evidence_literature NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_provenance.
- NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_assertion SIO_000772 14603332 NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_provenance.
- NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_assertion wasDerivedFrom befree-2016 NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_provenance.
- NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_assertion wasGeneratedBy ECO_0000203 NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_provenance.
- befree-2016 importedOn "2016-02-19" NP419552.RAVPUJXm5vDnwks_zdQSKsuDHkAXea9dJ2wgr-ulMTmBM130_provenance.