Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_provenance.
- NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_assertion description "[The phenotype of AR-DRD with the Leu205Pro mutation in the TH gene, which produces a severe decrease in TH activity to 1.5% of that of the wild type, was severe, not dystonia/Segawa's syndrome, but early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_provenance.
- NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_assertion evidence source_evidence_literature NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_provenance.
- NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_assertion SIO_000772 10661862 NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_provenance.
- NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_assertion wasDerivedFrom befree-20150227 NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_provenance.
- NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_assertion wasGeneratedBy ECO_0000203 NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP735244.RARnUQlmHEKe0vcH-6RCVfNHrpnVe1jcM7fnuzPjSlt2w130_provenance.