Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_assertion> ?p ?o ?g. }
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- NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_assertion type Assertion NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_head.
- NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_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." NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_provenance.
- NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_assertion evidence source_evidence_literature NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_provenance.
- NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_assertion SIO_000772 23559859 NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_provenance.
- NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_assertion wasDerivedFrom befree-2016 NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_provenance.
- NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_assertion wasGeneratedBy ECO_0000203 NP1066782.RA1V3yBLPQrHvi65EOHMZsLQZvrSaNvXrEozlGJUXg9Rc130_provenance.