@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_head { this: np:hasAssertion dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_assertion; np:hasProvenance dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_provenance; np:hasPublicationInfo dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_publicationInfo; a np:Nanopublication . dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_assertion a np:Assertion . dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_provenance a np:Provenance . dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_publicationInfo a np:PublicationInfo . } dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_assertion { miriam-gene:1740 a ncit:C16612 . lld:C0030567 a ncit:C7057 . dgn-gda:DGN7254535dbe5989ac23a8d960452e6a82 sio:SIO_000628 miriam-gene:1740, lld:C0030567; a sio:SIO_001122 . } dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_provenance { dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_assertion dcterms:description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:17052657; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP103295.RAcsv4EP4_CRjbyDemK7gRoQHc5rXxGvVwV9Jk3C_NxEg130_publicationInfo { this: dcterms:created "2016-05-13T12:42:34+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }