Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_provenance.
- NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_assertion description "[Rapid-onset dystonia-parkinsonism (RDP, DYT12) is a distinctive autosomal-dominant movement disorder with variable expressivity and reduced penetrance characterized by abrupt onset of dystonia, usually accompanied by signs of parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_provenance.
- NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_assertion evidence source_evidence_literature NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_provenance.
- NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_assertion SIO_000772 15260953 NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_provenance.
- NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_assertion wasDerivedFrom befree-20150227 NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_provenance.
- NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_assertion wasGeneratedBy ECO_0000203 NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256148.RAc-qSdoTNoOop-bRS4DYeXns7LU4m1-5nT8VBE-4E_1Y130_provenance.