Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_provenance.
- NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_assertion description "[The MLL gene rearrangements were found in 6.6% of patients, the -5/?5q- and/?or -7/?7q- aberrations in 7.7% of patients, while the most frequent genetic abnormality in our study was trisomy 8 (10%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_provenance.
- NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_assertion evidence source_evidence_literature NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_provenance.
- NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_assertion SIO_000772 26299742 NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_provenance.
- NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_assertion wasDerivedFrom befree-2016 NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_provenance.
- NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_assertion wasGeneratedBy ECO_0000203 NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293085.RAn_RxvlMp79XCAIOQFMntEcQ1ZO-YIgffV6HVKWda848130_provenance.