Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_provenance.
- NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_assertion description "[A total of 358 consecutive del(5q) cases were identified; specific diagnoses included myelodysplastic syndrome (MDS; 53%), acute myeloid leukemia (AML; 22%), plasma cell proliferative disorder (PCPD; 9%), myeloproliferative disorder (MPD; 7%), acute lymphoblastic leukemia (ALL; 2%), PCPD with MDS (2%), MDS/MPD (2%), and malignant lymphoma (ML; 2%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_provenance.
- NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_assertion evidence source_evidence_literature NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_provenance.
- NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_assertion SIO_000772 17707907 NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_provenance.
- NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_assertion wasDerivedFrom befree-20140225 NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_provenance.
- NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_assertion wasGeneratedBy ECO_0000203 NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP791359.RAqQUZWqGMB0ZqOyIfZIUEevQhIHaJ9mVxLYdnxZel_t4130_provenance.