Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_provenance.
- befree-2016 importedOn "2016-02-19" NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_provenance.
- NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_assertion wasGeneratedBy ECO_0000203 NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_provenance.
- NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_assertion wasDerivedFrom befree-2016 NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_provenance.
- NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_assertion SIO_000772 10850866 NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_provenance.
- NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_assertion evidence source_evidence_literature NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_provenance.
- NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_assertion description "[Primary glioblastomas are characterized by EGFR amplification/overexpression, PTEN mutation, homozygous p16 deletion, and loss of heterozygosity (LOH) on entire chromosome 10, whereas secondary glioblastomas frequently contain p53 mutations and show LOH on chromosome 10q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286284.RACwqt1e7W0vc2ROCAJSA-qMdXZDUARZ-yUeM8PdSzo-8130_provenance.