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- source_evidence_literature type ECO_0000212 NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_provenance.
- NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_assertion description "[Both sequence alteration and frequent copy number aberration were detected in two TK genes (HCK and ERBB2), strongly suggesting that they encode potential oncogenes in GC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_provenance.
- NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_assertion evidence source_evidence_literature NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_provenance.
- NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_assertion SIO_000772 19734198 NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_provenance.
- NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_assertion wasDerivedFrom befree-20150227 NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_provenance.
- NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_assertion wasGeneratedBy ECO_0000203 NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP444990.RAK3PZS9CVRi4_bJ4jJ9J5VizBxHZicP4UZIfAG6R99pM130_provenance.