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- source_evidence_literature type ECO_0000212 NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_provenance.
- NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_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." NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_provenance.
- NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_assertion evidence source_evidence_literature NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_provenance.
- NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_assertion SIO_000772 24875472 NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_provenance.
- NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_assertion wasDerivedFrom befree-2016 NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_provenance.
- NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_assertion wasGeneratedBy ECO_0000203 NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1186692.RA7QBK83aTrBEq1Ntjk0yoTyjQ0NkmbJbgl-JoyRTxAdg130_provenance.