Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_provenance.
- NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_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." NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_provenance.
- NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_assertion evidence source_evidence_literature NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_provenance.
- NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_assertion SIO_000772 23770245 NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_provenance.
- NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_assertion wasDerivedFrom befree-2016 NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_provenance.
- NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_assertion wasGeneratedBy ECO_0000203 NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1086218.RARDNeiVcyl6rBMi0KtKYWGgMNMmU8rpxWPIS7kwwZMI8130_provenance.