Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_provenance.
- NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_assertion description "[Although the frequency of mutations in the p16/CDKN2 gene has been detected in approximately 30% of non-small cell lung cancer, loss of heterozygosity on 9p has been observed in greater than 70% of non-small cell lung cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_provenance.
- NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_assertion evidence source_evidence_literature NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_provenance.
- NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_assertion SIO_000772 8988029 NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_provenance.
- NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_assertion wasDerivedFrom befree-20140225 NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_provenance.
- NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_assertion wasGeneratedBy ECO_0000203 NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP540055.RAXnJzBK_Vj9UWJNsYCQhSUcbMfymGK2clQhMRbtfs6FQ130_provenance.