Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_assertion type Assertion NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_head.
- NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_assertion description "[Here, we show that homozygous mutant mice expressing p53?31, a p53 lacking the C-terminal domain, exhibit increased p53 activity and suffer from aplastic anemia and pulmonary fibrosis, hallmarks of syndromes caused by short telomeres.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_provenance.
- NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_assertion evidence source_evidence_literature NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_provenance.
- NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_assertion SIO_000772 23770245 NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_provenance.
- NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_assertion wasDerivedFrom befree-20150227 NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_provenance.
- NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_assertion wasGeneratedBy ECO_0000203 NP751173.RA-cLlQfiKz3VltNZXj40G18gRMvdAyUpk8NuuFx7O1_M130_provenance.