http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#head http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#assertion http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#provenance http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#assertion http://rdf.disgenet.org/resource/gda/DGN7f790bbb2b421ff23f5a8d249a74c231 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/2643 http://rdf.disgenet.org/resource/gda/DGN7f790bbb2b421ff23f5a8d249a74c231 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0393593 http://rdf.disgenet.org/resource/gda/DGN7f790bbb2b421ff23f5a8d249a74c231 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#provenance http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#assertion http://purl.org/dc/terms/description [Hereditary Progressive Dystonia with marked diurnal fluctuation (HPD) is an autosomally dominantly inherited dystonia which is characterized by marked diurnal fluctuation of symptoms and by marked and sustained response to levodopa associated with mutations in guanosine triphosphate cyclohydrolase (GCH-1) deficiency gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#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/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/15959854 http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#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/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/dc/terms/created 2017-10-17T13:12:56+02:00 http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP433803.RAw-nci0wvP1XOfsAKzBJiMRnXTZQfsVeqNF7PiuV6Ba8 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