@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:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_head { this: np:hasAssertion dgn-np:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_assertion; np:hasProvenance dgn-np:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_provenance; np:hasPublicationInfo dgn-np:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_assertion a np:Assertion . dgn-np:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_provenance a np:Provenance . dgn-np:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_assertion { miriam-gene:10133 a ncit:C16612 . lld:C0339573 a ncit:C7057 . dgn-gda:DGNbabb88c4f56038a99fd250a714fcc33f sio:SIO_000628 miriam-gene:10133, lld:C0339573; a sio:SIO_001121 . } dgn-np:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_provenance { dgn-np:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_assertion dcterms:description "[Optineurin, a cytosolic protein associated with the actin cytoskeleton, microtubules, and the Golgi complex, appears to have an important function in neurons, as mutations in its gene are causative for neurodegenerative diseases such as primary open-angle glaucoma and amyotrophic lateral sclerosis.]. 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:25096716; 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:NP1208089.RAQa1uBM63RBi8ncqxGFPR4Ni2blqjEccBjKaZr2l6TQQ130_publicationInfo { this: dcterms:created "2016-05-13T12:50:53+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" . }