Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_assertion> ?p ?o ?g. }
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- NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_assertion type Assertion NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_head.
- NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_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." NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_provenance.
- NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_assertion evidence source_evidence_literature NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_provenance.
- NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_assertion SIO_000772 20591486 NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_provenance.
- NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_assertion wasDerivedFrom gad-20150221 NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_provenance.
- NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_assertion wasGeneratedBy ECO_0000203 NP127295.RAayMCaZTwLQTbiPXGqSUBOIceRmS-h0nlncK1jooT8Sc130_provenance.