Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_assertion> ?p ?o ?g. }
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- NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_assertion type Assertion NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_head.
- NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_assertion description "[In this study, we have applied 250K SNP array technology to detect previously cryptic chromosomal changes, particularly UPD, in a cohort of 301 patients with myelodysplastic syndromes (MDS), overlap MDS/myeloproliferative disorders (MPD), MPD, and acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_provenance.
- NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_assertion evidence source_evidence_literature NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_provenance.
- NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_assertion SIO_000772 19074904 NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_provenance.
- NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_assertion wasDerivedFrom befree-20140225 NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_provenance.
- NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_assertion wasGeneratedBy ECO_0000203 NP922720.RAlB_n-iDedDze06Aa63L96Wa3gM2C8nShAHqH5qIIFO0130_provenance.