Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_provenance.
- NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_assertion wasGeneratedBy ECO_0000203 NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_provenance.
- NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_assertion wasDerivedFrom befree-20150227 NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_provenance.
- NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_assertion SIO_000772 23144630 NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_provenance.
- NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_assertion evidence source_evidence_literature NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_provenance.
- NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_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." NP595038.RARMLeHhWjWzw73lc1kDFNsjeaYv9NKZzas5uVXNuYwX4130_provenance.