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- source_evidence_literature type ECO_0000212 NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_provenance.
- NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_assertion description "[Demonstration of the MYD88 L265 mutation is a valuable tool for the diagnosis of LPL, although some SMZL cases carrying the mutation do not fulfill the diagnostic criteria for LPL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_provenance.
- NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_assertion evidence source_evidence_literature NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_provenance.
- NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_assertion SIO_000772 25723115 NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_provenance.
- NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_assertion wasDerivedFrom befree-2016 NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_provenance.
- NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_assertion wasGeneratedBy ECO_0000203 NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266742.RA4io2L5U-wj6rgBGW_zpj7FYzveni41AVjrbAl72WikI130_provenance.