Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_assertion> ?p ?o ?g. }
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- NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_assertion type Assertion NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_head.
- NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_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." NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_provenance.
- NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_assertion evidence source_evidence_literature NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_provenance.
- NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_assertion SIO_000772 23770245 NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_provenance.
- NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_assertion wasDerivedFrom befree-20150227 NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_provenance.
- NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_assertion wasGeneratedBy ECO_0000203 NP749365.RANHgDTKoPN3FIUZSl0QiTYxsSDY4AfTn0xoV6JfBLy7s130_provenance.