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- source_evidence_literature type ECO_0000212 NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_provenance.
- NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_assertion description "[In a population-based patient cohort, SPIBhigh/BATFlow-ABC-DLBCL is enriched for mutation of MYD88, and SPIBhigh/BATFlow-ABC-DLBCL with MYD88-L265P mutation identifies a small subgroup of patients among this otherwise aggressive disease subgroup with distinct favourable outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_provenance.
- NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_assertion evidence source_evidence_literature NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_provenance.
- NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_assertion SIO_000772 24875472 NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_provenance.
- NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_assertion wasDerivedFrom befree-20150227 NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_provenance.
- NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_assertion wasGeneratedBy ECO_0000203 NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583079.RAY3ZXb6NonCbxlbuQxONKdP64OcdruACX93gZ480JguU130_provenance.