Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_provenance.
- NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_assertion description "[Among myeloid-BC, CD34-negative cases were more often associated with trisomy-8, 17p-loss and numerical abnormalities, and the CD117-negative subset with additional copies of Ph (p<0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_provenance.
- NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_assertion evidence source_evidence_literature NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_provenance.
- NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_assertion SIO_000772 18760473 NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_provenance.
- NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_assertion wasDerivedFrom befree-2016 NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_provenance.
- NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_assertion wasGeneratedBy ECO_0000203 NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_provenance.
- befree-2016 importedOn "2016-02-19" NP690832.RAD2FdgBcMcD1kI_D_T86PvcgbvGF8JsdTqAqdN5m9ruM130_provenance.