Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion type Assertion NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_head.
- NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion wasGeneratedBy ECO_0000203 NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_provenance.
- NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion wasDerivedFrom befree-20140225 NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_provenance.
- NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion SIO_000772 14732922 NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_provenance.
- NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion evidence source_evidence_literature NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_provenance.
- NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion description "[Because previous studies have shown that loss of heterozygosity (LOH) is common on chromosome arm 9p in esophageal squamous cell carcinoma (ESCC) and that genetic alterations in CDKN2A and CDKN2B on 9p are also common, we sought to determine whether LOH and these genetic alterations are related.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_provenance.