Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_assertion type Assertion NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_head.
- NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_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." NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_provenance.
- NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_assertion evidence source_evidence_literature NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_provenance.
- NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_assertion SIO_000772 20591486 NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_provenance.
- NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_assertion wasDerivedFrom gad-20150221 NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_provenance.
- NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_assertion wasGeneratedBy ECO_0000203 NP150443.RAuu-ZwWj4XIFK829EiKdbCP3eg-lOXRVUlYELmZqtOac130_provenance.