Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_assertion> ?p ?o ?g. }
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- NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_assertion type Assertion NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_head.
- NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_assertion wasGeneratedBy ECO_0000203 NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_provenance.
- NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_assertion wasDerivedFrom befree-20150227 NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_provenance.
- NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_assertion SIO_000772 20085575 NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_provenance.
- NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_assertion evidence source_evidence_literature NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_provenance.
- NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_assertion description "[The most frequent cytogenetic abnormalities were ETV6/RUNX1 fusion (16%) and trisomy 8 (14.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387322.RAtKW4PZtIQZqmsNi3rT0CnBczxEH78tGyfZmXB4QcN40130_provenance.