Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_provenance.
- NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_assertion description "[We describe here a family with blue cone monochromacy due to the presence of the C203R mutation in both RCP and GCP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_provenance.
- NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_assertion evidence source_evidence_literature NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_provenance.
- NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_assertion SIO_000772 8666378 NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_provenance.
- NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_assertion wasDerivedFrom befree-20140225 NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_provenance.
- NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_assertion wasGeneratedBy ECO_0000203 NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP801460.RAU9bV5EGa6-_NlAKWWQhwHqOht-ZTY24m8zmUdFmN-EQ130_provenance.