Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_provenance.
- NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_assertion description "[Our data show that molecular deletions of 13q14 are detected in a relatively large fraction of BCR/ABL- CMPD (38%), that they appear to be more frequent in MMM than in other BCR/ABL- CMPD, and that they may be present at diagnosis or occur during blastic evolution of the neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_provenance.
- NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_assertion evidence source_evidence_literature NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_provenance.
- NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_assertion SIO_000772 8527391 NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_provenance.
- NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_assertion wasDerivedFrom befree-20150227 NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_provenance.
- NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_assertion wasGeneratedBy ECO_0000203 NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP219632.RA2ZmpKxXz6Vp5QP4DCztp0at0hUATDmc8r_9Vj807frw130_provenance.