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- source_evidence_literature type ECO_0000212 NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_provenance.
- NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_assertion description "[These results suggest that STX11 gene mutations may be associated with secondary malignancies (MDS/AML), and that there is segregation of specific clinical features in FHL patients with an underlying genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_provenance.
- NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_assertion evidence source_evidence_literature NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_provenance.
- NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_assertion SIO_000772 16582076 NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_provenance.
- NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_assertion wasDerivedFrom befree-20140225 NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_provenance.
- NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_assertion wasGeneratedBy ECO_0000203 NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_provenance.