Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_provenance.
- NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_assertion description "[Heterozygous point mutations at Y641 and A677 in the EZH2 SET domain are prevalent in about 10-24% of Non-Hodgkin lymphomas (NHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_provenance.
- NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_assertion evidence source_evidence_literature NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_provenance.
- NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_assertion SIO_000772 22850114 NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_provenance.
- NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_assertion wasDerivedFrom befree-20140225 NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_provenance.
- NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_assertion wasGeneratedBy ECO_0000203 NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP711051.RAYDKm3AQ2wPSMaN-xATPUx42LD2STU2IckeLTVJenURY130_provenance.