Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_provenance.
- NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_assertion wasGeneratedBy ECO_0000203 NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_provenance.
- NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_assertion wasDerivedFrom befree-2016 NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_provenance.
- NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_assertion SIO_000772 23222563 NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_provenance.
- NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_assertion evidence source_evidence_literature NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_provenance.
- NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_assertion description "[Signalling pathways known to be disrupted in UM include: (1) the retinoblastoma pathway, probably as a result of cyclin D1 overexpression; p53 signalling, possibly as a consequence of MDM2 overexpression; and the P13K/AKT and mitogen-activated protein kinase/extracellular signal-related kinase pathway pathways that are disturbed as a result of PTEN and GNAQ/11 mutations, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1034384.RAbYyZZy_SU_l2CqFaJ5XGjs6gkZc0MjIQpdc319UYl0o130_provenance.