Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_assertion> ?p ?o ?g. }
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- NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_assertion type Assertion NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_head.
- NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_assertion wasGeneratedBy ECO_0000203 NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_provenance.
- NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_assertion wasDerivedFrom befree-20140225 NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_provenance.
- NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_assertion SIO_000772 20013787 NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_provenance.
- NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_assertion evidence source_evidence_literature NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_provenance.
- NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_assertion description "[WT1 mutations occur in approximately 10% of adult AML patients at diagnosis and are most frequent in the cytogenetically normal (CN) AML subgroup.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692825.RAdGKgraNmzUDJgR0JipLmbg-8AQx4c_KXHug84ExljL0130_provenance.