http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#head http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#assertion http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#provenance http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#assertion http://rdf.disgenet.org/resource/gda/DGN712240c672d5a77a579ef59273789833 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/51142 http://rdf.disgenet.org/resource/gda/DGN712240c672d5a77a579ef59273789833 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C3489791 http://rdf.disgenet.org/resource/gda/DGN712240c672d5a77a579ef59273789833 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#provenance http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#assertion http://purl.org/dc/terms/description [Further genetic studies in other populations are needed to confirm the pathogenicity of CHCHD2 mutations in autosomal dominant Parkinson's disease and susceptibility for sporadic Parkinson's disease, and further functional studies are needed to understand how mutant CHCHD2 might play a part in the pathophysiology of Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#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/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/25662902 http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#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/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/dc/terms/created 2017-10-17T13:18:30+02:00 http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1307477.RAinwnvshVNbG4VZndcp6WytYwYRaPZ4F6yMG45GTf0zk 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