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- source_evidence_literature type ECO_0000212 NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_provenance.
- NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_provenance.
- NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_assertion evidence source_evidence_literature NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_provenance.
- NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_assertion SIO_000772 23357145 NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_provenance.
- NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_assertion wasDerivedFrom befree-2016 NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_provenance.
- NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_assertion wasGeneratedBy ECO_0000203 NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_provenance.