http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#head http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#assertion http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#provenance http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#assertion http://rdf.disgenet.org/resource/gda/DGN51c41c579580ae5c52b5852f790cd944 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/1861 http://rdf.disgenet.org/resource/gda/DGN51c41c579580ae5c52b5852f790cd944 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0393593 http://rdf.disgenet.org/resource/gda/DGN51c41c579580ae5c52b5852f790cd944 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#provenance http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#assertion http://purl.org/dc/terms/description [Moreover, dystonia and Parkinson disease share the common feature of reduced dopamine neurotransmission in the striatum, so we assumed that mutations in the DYT1 gene might have the same role in cases of early onset primary torsion dystonia (EOPTD) and early onset Parkinson disease (EOPD) that present dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/19038309 http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/dc/terms/created 2017-10-17T13:12:07+02:00 http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP305677.RA5IM8io01UEPqg6fTMZKCTmfUgEWFayj2jE_NouGAEik http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0