Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_provenance.
- NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_assertion description "[The use of reverse-transcription polymerase chain reaction (RT-PCR) for the detection of the PML-RARA and RARA-PML fusion genes is the only technique that defines the PML breakpoint type and that allows the definition of a correct strategy for subsequent minimal residual disease (MRD) monitoring.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_provenance.
- NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_assertion evidence source_evidence_literature NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_provenance.
- NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_assertion SIO_000772 16502581 NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_provenance.
- NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_assertion wasDerivedFrom befree-20140225 NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_provenance.
- NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_assertion wasGeneratedBy ECO_0000203 NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_provenance.
- befree-20140225 importedOn "2014-02-25" NP797390.RA5KSeyihKNGt8JJA90WbiTVUN-SY9MPpekNQ1xcEc5Js130_provenance.