Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_assertion> ?p ?o ?g. }
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- NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_assertion type Assertion NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_head.
- NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_assertion description "[Mutations in PRPF31, RHO, and PRPH2 were found in low frequencies (1 of 9 autosomal dominant RP families) in Chinese patients, and the PRPF31 and PRPH2 truncating mutations were novel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_provenance.
- NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_assertion evidence source_evidence_literature NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_provenance.
- NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_assertion SIO_000772 19506198 NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_provenance.
- NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_assertion wasDerivedFrom gad-20130706 NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_provenance.
- NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_assertion wasGeneratedBy ECO_0000203 NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_provenance.