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- source_evidence_literature type ECO_0000212 NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_provenance.
- NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_assertion description "[These coexistent mutations/epigenetic inactivations in PI3K/AKT pathway may be responsible for the unusually aggressive course of ACC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_provenance.
- NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_assertion evidence source_evidence_literature NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_provenance.
- NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_assertion SIO_000772 17669465 NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_provenance.
- NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_assertion wasDerivedFrom befree-20140225 NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_provenance.
- NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_assertion wasGeneratedBy ECO_0000203 NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_provenance.
- befree-20140225 importedOn "2014-02-25" NP811083.RAHrxqVxEobn-BuNc_effrBH_WIoFp5CSjkoElA3NmO78130_provenance.