Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_assertion type Assertion NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_head.
- NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_assertion description "[PTEN and NOTCH1 mutations were almost mutually exclusive, while IL7R and WT1 mutations were rare in pediatric T-ALL and PTPN11 and AKT1 mutations were infrequent in adult T-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_provenance.
- NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_assertion evidence source_evidence_literature NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_provenance.
- NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_assertion SIO_000772 26341754 NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_provenance.
- NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_assertion wasDerivedFrom befree-2016 NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_provenance.
- NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_assertion wasGeneratedBy ECO_0000203 NP1293736.RABAepvtMMOm_pdvVqzgx8CRidvARaXUwsxaDxgSBHC6o130_provenance.