Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_provenance.
- NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_assertion wasGeneratedBy ECO_0000203 NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_provenance.
- NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_assertion wasDerivedFrom befree-2016 NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_provenance.
- NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_assertion SIO_000772 23144630 NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_provenance.
- NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_assertion evidence source_evidence_literature NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_provenance.
- NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_assertion description "[In asymptomatic carriers CNOT3 is expressed at low levels, allowing higher amounts of wild-type PRPF31 transcripts to be produced and preventing manifestation of retinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1027736.RAYOtC22KD9LJQDNzl4KrRfT_nATBT-V6HOrwPVFLBGkQ130_provenance.