Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_assertion> ?p ?o ?g. }
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- NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_assertion type Assertion NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_head.
- NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_assertion wasGeneratedBy ECO_0000203 NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_provenance.
- NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_assertion wasDerivedFrom befree-2016 NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_provenance.
- NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_assertion SIO_000772 11566339 NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_provenance.
- NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_assertion evidence source_evidence_literature NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_provenance.
- NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_assertion description "[There were also frequently observed secondary changes such as chromosome 1 rearrangement leading to trisomy of 1q and loss of tp53 from the deleted chromosome 17.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330779.RACqVBdkqU9HDrJc_dpRXMULgSFzJnD190U5VueQY1uNM130_provenance.