Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_provenance.
- NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_assertion description "[Taken together, our results demonstrate the robust performance of VarScan 2 for somatic mutation and CNA detection and shed new light on the landscape of genetic alterations in ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_provenance.
- NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_assertion evidence source_evidence_literature NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_provenance.
- NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_assertion SIO_000772 22300766 NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_provenance.
- NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_assertion wasDerivedFrom befree-20140225 NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_provenance.
- NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_assertion wasGeneratedBy ECO_0000203 NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP650498.RAncFV7QLRYeq75NGcJ9pA2vE3T8Fn7JX9lfYHnIEasJI130_provenance.