@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:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_head { this: np:hasAssertion dgn-np:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_assertion; np:hasProvenance dgn-np:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_provenance; np:hasPublicationInfo dgn-np:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_publicationInfo; a np:Nanopublication . dgn-np:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_assertion a np:Assertion . dgn-np:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_provenance a np:Provenance . dgn-np:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_publicationInfo a np:PublicationInfo . } dgn-np:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_assertion { miriam-gene:120892 a ncit:C16612 . lld:C0030567 a ncit:C7057 . dgn-gda:DGNed72fba8c86ada1540358d418efa65c6 sio:SIO_000628 miriam-gene:120892, lld:C0030567; a sio:SIO_001121 . } dgn-np:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_provenance { dgn-np:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_assertion dcterms:description "[Sequence analysis of 29 exons coding for functional domains of LRRK2 in 160 nondominant Parkinson disease patients was performed/novel variants (R1067Q and IVS33 + 6 T > A) were found, which are likely to be pathogenic in five patients.]. 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:16247070; prov:wasDerivedFrom dgn-void:lhgdn-20090331; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP213782.RAV_-zCG5qpJWWRZe_UzyJYz8QgLqbz9cBgayXoCbXELU130_publicationInfo { this: dcterms:created "2016-05-13T12:43:23+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" . }