Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_provenance.
- NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_assertion description "[This may reflect the frequency of association of ABL gene and BCR gene abnormality in our cases, and that absence of fusion gene BCR/ABL does not exclude their role in the leukomogenic process, yet a larger study is required to confirm and detect the prevalence of these gene disturbances in ALL and their association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_provenance.
- NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_assertion evidence source_evidence_literature NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_provenance.
- NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_assertion SIO_000772 17496935 NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_provenance.
- NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_assertion wasDerivedFrom befree-20140225 NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_provenance.
- NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_assertion wasGeneratedBy ECO_0000203 NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP308876.RA5FMyYhxV_lIizFxWEXut_T6vaJF9ixlEglNxB1ydTWU130_provenance.