Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_assertion type Assertion NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_head.
- NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_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." NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_provenance.
- NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_assertion evidence source_evidence_literature NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_provenance.
- NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_assertion SIO_000772 20591486 NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_provenance.
- NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_assertion wasDerivedFrom gad-20150221 NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_provenance.
- NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_assertion wasGeneratedBy ECO_0000203 NP180174.RAO9euOBNpoZT63oKtNguCFhE4opa0vgSBryH-qOfDCXY130_provenance.