Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_provenance.
- NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_assertion description "[Appropriate oligoprimers complementary to PML and RAR-a sequences nearby the DNA breakpoints may be successfully used in PCR experiments to amplify the PML/RAR-a hybrid gene and sensitively detect minimal residual disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_provenance.
- NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_assertion evidence source_evidence_literature NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_provenance.
- NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_assertion SIO_000772 8180596 NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_provenance.
- NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_assertion wasDerivedFrom befree-20140225 NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_provenance.
- NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_assertion wasGeneratedBy ECO_0000203 NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP179076.RA5vU021EUzLEMI1drF81CKPD3MDmLukPvG6v7GT1CVrI130_provenance.