Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_provenance.
- NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_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." NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_provenance.
- NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_assertion evidence source_evidence_literature NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_provenance.
- NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_assertion SIO_000772 8666378 NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_provenance.
- NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_assertion wasDerivedFrom befree-20140225 NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_provenance.
- NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_assertion wasGeneratedBy ECO_0000203 NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP795777.RA2wtOy1FioGxKxFry30p4doMgg1HtHWuMYN1ZGuad0Cs130_provenance.