@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:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_head { this: np:hasAssertion dgn-np:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_assertion; np:hasProvenance dgn-np:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_provenance; np:hasPublicationInfo dgn-np:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_publicationInfo; a np:Nanopublication . dgn-np:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_assertion a np:Assertion . dgn-np:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_provenance a np:Provenance . dgn-np:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_publicationInfo a np:PublicationInfo . } dgn-np:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_assertion { miriam-gene:10133 a ncit:C16612 . lld:C0017601 a ncit:C7057 . dgn-gda:DGNa73059aeddaa809714e086d63eb63e0c sio:SIO_000628 miriam-gene:10133, lld:C0017601; a sio:SIO_001121 . } dgn-np:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_provenance { dgn-np:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_assertion dcterms:description "[Since NTG is reported to be the most common form of glaucoma in Japan, and to identify if the OPTN gene plays a role in POAG, the DNAs from 148 unrelated Japanese patients with NTG, 165 patients with POAG and 196 unrelated controls who were not suffering glaucoma were investigated by appropriate genotyping techniques.]. 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:12811537; 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:NP398513.RAf4zDTvj3kZC6xq1iH6wiVtFfiW3hiVZI3LmaMFScis0130_publicationInfo { this: dcterms:created "2016-05-13T12:44:46+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" . }