Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_provenance.
- NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_assertion description "[arrayCGH analysis revealed a cryptic deletion of the region 4q24 in all eight patients selected with myeloid malignancies (3 MDS, 1 AML and 4 MPN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_provenance.
- NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_assertion evidence source_evidence_literature NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_provenance.
- NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_assertion SIO_000772 23389918 NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_provenance.
- NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_assertion wasDerivedFrom befree-20150227 NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_provenance.
- NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_assertion wasGeneratedBy ECO_0000203 NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP953854.RAO72W9uXPSS9Si5OPt5Qw71Cu8agST8l3YnTg3Jdr5nE130_provenance.