Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_provenance.
- NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_assertion wasGeneratedBy ECO_0000203 NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_provenance.
- NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_assertion wasDerivedFrom befree-20150227 NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_provenance.
- NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_assertion SIO_000772 23144630 NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_provenance.
- NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_assertion evidence source_evidence_literature NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_provenance.
- NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_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." NP881918.RA-cdH4mipIEnek_KhDgwYKaHxh_oxB28QDFk5tNxdMpo130_provenance.