@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:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_head { this: np:hasAssertion dgn-np:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_assertion; np:hasProvenance dgn-np:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_provenance; np:hasPublicationInfo dgn-np:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_publicationInfo; a np:Nanopublication . dgn-np:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_assertion a np:Assertion . dgn-np:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_provenance a np:Provenance . dgn-np:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_publicationInfo a np:PublicationInfo . } dgn-np:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_assertion { miriam-gene:120892 a ncit:C16612 . lld:C0030567 a ncit:C7057 . dgn-gda:DGNbbc16ed3a8bb9a56cc4215022fbff725 sio:SIO_000628 miriam-gene:120892, lld:C0030567; a sio:SIO_001122 . } dgn-np:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_provenance { dgn-np:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_assertion dcterms:description "[To evaluate the frequency of the LRRK2 P755L variant in North American Caucasian patients with PD, we screened 426 PD patients and 37 additional patients with the combination of PD and essential tremor (ET) from our Parkinson Disease Center and Movement Clinic at Baylor College of Medicine.]. 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:17482357; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP608327.RABJWpArQsXP2mHKmzNJaTZILQJyJ4k-Ib8Y6113uJ9so130_publicationInfo { this: dcterms:created "2016-05-13T12:46:21+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" . }