Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_assertion> ?p ?o ?g. }
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- NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_assertion type Assertion NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_head.
- NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_assertion wasGeneratedBy ECO_0000203 NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_provenance.
- NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_assertion wasDerivedFrom lhgdn-20090331 NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_provenance.
- NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_assertion SIO_000772 11875049 NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_provenance.
- NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_assertion evidence source_evidence_literature NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_provenance.
- NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_assertion description "[This mutant isoenzyme maps to human chromosome region 7q and has an amino acid substitution (arginine for proline)/is involved in the etiology of autosomal dominant retinitis pigmentosa in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122283.RAKQhIleUukJUV9chDbI-Nm1_23onmcxxoT58ebC9cUvw130_provenance.