@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:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_head { this: np:hasAssertion dgn-np:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_assertion; np:hasProvenance dgn-np:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_provenance; np:hasPublicationInfo dgn-np:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_assertion a np:Assertion . dgn-np:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_provenance a np:Provenance . dgn-np:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_assertion { miriam-gene:3075 a ncit:C16612 . lld:C0242383 a ncit:C7057 . dgn-gda:DGNb536c9e5b2dd6896180af24587a6eee5 sio:SIO_000628 miriam-gene:3075, lld:C0242383; a sio:SIO_001122 . } dgn-np:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_provenance { dgn-np:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_assertion dcterms:description "[The presence or absence of RPD was studied among 408 patients with exudative AMD in at least one eye, and the clinical characteristics of those with RPD were investigated as well as genetic polymorphisms of ARMS2 A69S (rs10490924) and CFH I62V (rs800292).]. 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:24595987; 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:NP1160470.RA1VJpjm6humCLJVQMCukRFlIPR5BDF2at9g91QEQ6NXQ130_publicationInfo { this: dcterms:created "2016-05-13T12:50:32+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" . }