Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_provenance.
- NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_assertion description "[A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_provenance.
- NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_assertion evidence source_evidence_literature NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_provenance.
- NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_assertion SIO_000772 9810570 NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_provenance.
- NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_assertion wasDerivedFrom befree-20150227 NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_provenance.
- NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_assertion wasGeneratedBy ECO_0000203 NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP649189.RAdcShUGM3T5tnRWbGusS8TqFPu-muZxmFDoT4mDonzK4130_provenance.