@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:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_head { this: np:hasAssertion dgn-np:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_assertion; np:hasProvenance dgn-np:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_provenance; np:hasPublicationInfo dgn-np:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_publicationInfo; a np:Nanopublication . dgn-np:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_assertion a np:Assertion . dgn-np:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_provenance a np:Provenance . dgn-np:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_publicationInfo a np:PublicationInfo . } dgn-np:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_assertion { miriam-gene:3075 a ncit:C16612 . lld:C0242383 a ncit:C7057 . dgn-gda:DGN4993ee3bbff0b0a4c8c4754178582a9c sio:SIO_000628 miriam-gene:3075, lld:C0242383; a sio:SIO_001121 . } dgn-np:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_provenance { dgn-np:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_assertion dcterms:description "[In fact, the main genetic changes (polymorphism) associated with AMD were found to be genes that regulate inflammation, most notably complement Factor H. This review ties together many studies done over the past decade to give us new insight into the role inflammation plays in the development of AMD.]. 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:21609232; 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:NP896513.RAAqFpv1EkR4C91ZwP7DPRtCQanQr2nfqFDVHSmoBu6Ho130_publicationInfo { this: dcterms:created "2016-05-13T12:48:30+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" . }