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- source_evidence_literature type ECO_0000212 NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_provenance.
- NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_assertion description "[In conclusion, the presence of mutation at codon 12 of the N-ras gene might serve as a negative prognostic factor at diagnosis of MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_provenance.
- NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_assertion evidence source_evidence_literature NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_provenance.
- NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_assertion SIO_000772 9031609 NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_provenance.
- NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_assertion wasDerivedFrom befree-20150227 NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_provenance.
- NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_assertion wasGeneratedBy ECO_0000203 NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP598664.RASsURe_9Ehxn88NYxtxJfbr4rqK2KeFkqFyBgIGXYfyE130_provenance.