Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion type Assertion NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_head.
- NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion wasGeneratedBy ECO_0000203 NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_provenance.
- NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion wasDerivedFrom befree-20140225 NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_provenance.
- NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion SIO_000772 11550302 NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_provenance.
- NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion evidence source_evidence_literature NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_provenance.
- NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_assertion description "[Loss of 9p or homozygous deletion of the CDKN2 gene or both are associated with anaplastic oligodendrogliomas, whereas loss of 17p or TP53 gene mutations or both are frequent in astrocytomas, but rare in oligodendrogliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911236.RA0CsbpdPBj0RVAZkfE1wJrr_emwiQUM47pxCZYTcoS6A130_provenance.