Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_assertion type Assertion NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_head.
- NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_assertion description "[The most common chromosome abnormality found in this tumor is loss of heterozygosity (LOH) on the short arm of chromosome 3, which suggests that there must be one or more tumor suppressor genes between 3p14 and 3p21 near the VHL gene which play a relevant role in renal cancer development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_provenance.
- NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_assertion evidence source_evidence_literature NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_provenance.
- NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_assertion SIO_000772 10971171 NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_provenance.
- NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_assertion wasDerivedFrom befree-2016 NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_provenance.
- NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_assertion wasGeneratedBy ECO_0000203 NP293993.RAAG-kzRBncQOStxcPfTY2lxyZ4-0EF30R5vIg6Esibd4130_provenance.