Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_assertion> ?p ?o ?g. }
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- NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_assertion type Assertion NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_head.
- NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in a]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_provenance.
- NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_assertion evidence source_evidence_literature NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_provenance.
- NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_assertion SIO_000772 20591486 NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_provenance.
- NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_assertion wasDerivedFrom gad-20150221 NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_provenance.
- NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_assertion wasGeneratedBy ECO_0000203 NP180189.RAnkFreL613sEC1nYSrn6E5YTVTnmQa7RiR1XyAi3fk0w130_provenance.