Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_assertion type Assertion NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_head.
- NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_assertion description "[To devise an effective method for detecting mutations in 12 genes (CA4, CRX, IMPDH1, NR2E3, RP9, PRPF3, PRPF8, PRPF31, PRPH2, RHO, RP1, and TOPORS) commonly associated with autosomal dominant retinitis pigmentosa (adRP) that account for more than 95% of known mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_provenance.
- NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_assertion evidence source_evidence_literature NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_provenance.
- NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_assertion SIO_000772 23559859 NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_provenance.
- NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_assertion wasDerivedFrom befree-2016 NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_provenance.
- NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_assertion wasGeneratedBy ECO_0000203 NP1066783.RAVAw-vxCDk-M3sWND2BfLu92CnLhZATem7IIULY77lEk130_provenance.