Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_assertion type Assertion NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_head.
- NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_assertion wasGeneratedBy ECO_0000203 NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_provenance.
- NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_assertion wasDerivedFrom befree-20140225 NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_provenance.
- NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_assertion SIO_000772 22619094 NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_provenance.
- NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_assertion evidence source_evidence_literature NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_provenance.
- NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_assertion description "[The aim of this study was to determine whether CLL patients with isolated trisomy 12 or associated with other chromosomal alterations have different clinico-pathological features, including a different distribution NOTCH1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505805.RAfPEFdJ8T3GXixlBLXh1yfH664NElmdtevjGbgrcrOmc130_provenance.