Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_assertion> ?p ?o ?g. }
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- NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_assertion type Assertion NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_head.
- NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_assertion description "[These data suggest that potentially pathogenic ROM1 mutations occur in 1% or less of patients with adRP or simplex RP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_provenance.
- NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_assertion evidence source_evidence_literature NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_provenance.
- NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_assertion SIO_000772 8595413 NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_provenance.
- NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_assertion wasDerivedFrom befree-20150227 NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_provenance.
- NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_assertion wasGeneratedBy ECO_0000203 NP674099.RAdNl7Zs5hrFt9WtbJxU0a40-VRMD68mySNF6ic4UGK7E130_provenance.