@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:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_head { this: np:hasAssertion dgn-np:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_assertion; np:hasProvenance dgn-np:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_provenance; np:hasPublicationInfo dgn-np:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_publicationInfo; a np:Nanopublication . dgn-np:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_assertion a np:Assertion . dgn-np:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_provenance a np:Provenance . dgn-np:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_publicationInfo a np:PublicationInfo . } dgn-np:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_assertion { miriam-gene:7422 a ncit:C16612 . lld:C0242383 a ncit:C7057 . dgn-gda:DGN939c416badd3e634007202e27159e8b3 sio:SIO_000628 miriam-gene:7422, lld:C0242383; a sio:SIO_001121 . } dgn-np:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_provenance { dgn-np:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_assertion dcterms:description "[Drugs targeting complement and vascular endothelial growth factor (VEGF) systems are under evaluation, and forthcoming work on rare variants and noncoding DNA in AMD pathogenesis will likely reveal biochemical pathways enriched with AMD-associated genetic variants.]. 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:25125423; 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:NP1210944.RAUuqPWqGpzPJB1SzZusHKCKKDS7E3AjI0XLMLAxa933E130_publicationInfo { this: dcterms:created "2016-05-13T12:50:54+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" . }