Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_assertion> ?p ?o ?g. }
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- NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_assertion type Assertion NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_head.
- NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_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." NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_provenance.
- NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_assertion evidence source_evidence_literature NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_provenance.
- NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_assertion SIO_000772 20591486 NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_provenance.
- NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_assertion wasDerivedFrom gad-20150221 NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_provenance.
- NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_assertion wasGeneratedBy ECO_0000203 NP65171.RAjbkjNjkLDKm9BjsaRG_ORe-o4a0LIDD7ZJf-HQ2rllI130_provenance.