Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_provenance.
- NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_assertion description "[Here we report that high-grade serous ovarian cancer is characterized by TP53 mutations in almost all tumours (96%); low prevalence but statistically recurrent somatic mutations in nine further genes including NF1, BRCA1, BRCA2, RB1 and CDK12; 113 significant focal DNA copy number aberrations; and promoter methylation events involving 168 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_provenance.
- NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_assertion evidence source_evidence_literature NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_provenance.
- NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_assertion SIO_000772 21720365 NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_provenance.
- NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_assertion wasDerivedFrom befree-20150227 NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_provenance.
- NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_assertion wasGeneratedBy ECO_0000203 NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP908576.RAoF8pfeWmouwqts3PZeZiJVW1Nd9eGGnWbn-R7NJTMpk130_provenance.