Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_provenance.
- NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_assertion description "[Mutations in the peripherin/retinal degeneration slow (RDS) gene are a known cause of various types of central retinal dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_provenance.
- NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_assertion evidence source_evidence_literature NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_provenance.
- NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_assertion SIO_000772 17653047 NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_provenance.
- NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_assertion wasDerivedFrom befree-2016 NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_provenance.
- NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_assertion wasGeneratedBy ECO_0000203 NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_provenance.
- befree-2016 importedOn "2016-02-19" NP621700.RAuBTx-PiPfJ-Dx6VV6pAnJKIOKB5oBmlouar6exmRTqI130_provenance.