http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#head http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#assertion http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#provenance http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#assertion http://rdf.disgenet.org/resource/gda/DGN78858099ba495e2a9e8cf29b5427738a http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/120892 http://rdf.disgenet.org/resource/gda/DGN78858099ba495e2a9e8cf29b5427738a http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0085084 http://rdf.disgenet.org/resource/gda/DGN78858099ba495e2a9e8cf29b5427738a http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#provenance http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#assertion http://purl.org/dc/terms/description [Mutations in leucine-rich repeat kinase 2 gene (PARK8/LRRK2) encoding the protein Lrrk2 are causative of inherited and sporadic Parkinson's disease (PD) with phenotypic manifestations of frontotemporal lobar degeneration, corticobasal degeneration and associated motor neuron disease in some patients, and with variable penetrance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#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/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/19142648 http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#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/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/dc/terms/created 2017-10-17T13:19:05+02:00 http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1400749.RA61cvn7evfxxRYHVGDa36GqaoBm61ofI-fD1_h7jegYo 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