Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_provenance.
- NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_assertion description "[We internally and externally validated a subset of 11 cluster II (poor prognosis)-specific genes having corresponding chromosomal aberrations identified by comparative genomic hybridization as prognostic markers in an independent cohort of patients with lung squamous cell carcinoma identifying CSNK2A1 and C1-Inh as independent predictors of outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_provenance.
- NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_assertion evidence source_evidence_literature NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_provenance.
- NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_assertion SIO_000772 15355908 NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_provenance.
- NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_assertion wasDerivedFrom befree-2016 NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_provenance.
- NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_assertion wasGeneratedBy ECO_0000203 NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_provenance.
- befree-2016 importedOn "2016-02-19" NP459064.RAe0pD_1sLMxnL6rAVpQPN7nsSGdH994MycnG2uELNxoE130_provenance.