Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_provenance.
- NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_assertion description "[Patients with the dystonia plus syndrome DYT5 display levodopa-responsive dystonia sometimes associated with tremor or parkinsonism (DYT5a, mutations in GCH1); a more severe phenotype with psychomotor involvement can be seen in recessive forms (DYT5b with TH mutations, SPR-deficiency syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_provenance.
- NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_assertion evidence source_evidence_literature NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_provenance.
- NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_assertion SIO_000772 22166420 NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_provenance.
- NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_assertion wasDerivedFrom befree-20150227 NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_provenance.
- NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_assertion wasGeneratedBy ECO_0000203 NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_provenance.
- befree-20150227 importedOn "2015-02-27" NP735401.RAD8f-VNRQCJHtHLfnUDH1FqX7YxLLfVsYAaiXM6Cyqko130_provenance.