Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_provenance.
- 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.
- gad-20130706 importedOn "2013-07-06" NP52353.RAqWMBymzqXIuZ0vIHPeX51Ptcnn73I2-CUPWjcXwVndE130_provenance.