Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_provenance.
- NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_assertion wasGeneratedBy ECO_0000203 NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_provenance.
- NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_assertion wasDerivedFrom befree-20150227 NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_provenance.
- NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_assertion SIO_000772 23335386 NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_provenance.
- NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_assertion evidence source_evidence_literature NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_provenance.
- NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_assertion description "[We conclude that SRSF2 is the most frequently mutated spliceosome gene in CMML but neither it nor SF3B1 or U2AF35 mutations are prognostically relevant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873159.RAjJoxuLAhxv1slL9UULU9yWCdXK_RwsqQTOC3jTcG8uM130_provenance.