Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_provenance.
- NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_assertion description "[In addition, we suggest that der(17)t(12;17)(q13;p13) should be considered a new recurrent, nonrandom chromosomal abnormality in patients with t-MDS/AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_provenance.
- NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_assertion evidence source_evidence_literature NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_provenance.
- NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_assertion SIO_000772 19155067 NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_provenance.
- NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_assertion wasDerivedFrom befree-20140225 NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_provenance.
- NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_assertion wasGeneratedBy ECO_0000203 NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP258224.RAEuC9-ODm7T7KsRfCs8Tu1W7K5vLGRWwIa7IpZGGOomA130_provenance.