Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_provenance.
- NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_assertion description "[We have studied hypermethylation of the PTEN promoter, loss of heterozygosity (LOH) at microsatellites in chromosome 10q23 (surrounding and intragenic to the PTEN locus), and hypermethylation of PTEN's highly homologous pseudogene, PTENP1, and their association with PTEN protein loss in a surgical case series study of primary NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_provenance.
- NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_assertion evidence source_evidence_literature NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_provenance.
- NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_assertion SIO_000772 16084946 NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_provenance.
- NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_assertion wasDerivedFrom befree-20140225 NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_provenance.
- NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_assertion wasGeneratedBy ECO_0000203 NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478208.RA5YGwB5XpeclGHYjh1xjRi9chJ47CXYgJpBGRL3asV20130_provenance.