Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_assertion type Assertion NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_head.
- NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_assertion description "[Existence of the P16INK4A mutation and the hereditary TP53 mutation with or without loss of heterozygosity in the TP53 gene (seminoma/medulloblastoma) may be evidence for a common mechanism involved in tumorogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_provenance.
- NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_assertion evidence source_evidence_literature NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_provenance.
- NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_assertion SIO_000772 10484981 NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_provenance.
- NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_assertion wasDerivedFrom befree-2016 NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_provenance.
- NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_assertion wasGeneratedBy ECO_0000203 NP262877.RAUwZtKW73lMxLnn3OpUWDqe48qfH92BFXqD6D2Ggg26A130_provenance.