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- source_evidence_literature type ECO_0000212 NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_provenance.
- NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_assertion wasGeneratedBy ECO_0000203 NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_provenance.
- NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_assertion wasDerivedFrom lhgdn-20090331 NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_provenance.
- NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_assertion SIO_000772 11875049 NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_provenance.
- NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_assertion evidence source_evidence_literature NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_provenance.
- NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_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." NP193491.RAH-o-TuG7U3D6Oo0xs8hxK7L-Eo9kTj4kjStCnXlH15M130_provenance.