@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:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_head { this: np:hasAssertion dgn-np:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_assertion; np:hasProvenance dgn-np:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_provenance; np:hasPublicationInfo dgn-np:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_publicationInfo; a np:Nanopublication . dgn-np:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_assertion a np:Assertion . dgn-np:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_provenance a np:Provenance . dgn-np:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_publicationInfo a np:PublicationInfo . } dgn-np:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_assertion { miriam-gene:19 a ncit:C16612 . lld:C0242383 a ncit:C7057 . dgn-gda:DGNf7734868f4d779ddee0ef74e30e0c406 sio:SIO_000628 miriam-gene:19, lld:C0242383; a sio:SIO_001121 . } dgn-np:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_provenance { dgn-np:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_assertion dcterms:description "[A total of 24 variants from five genes (BCMO1, BCO2, NPCL1L1, ABCG8, and FADS2) not previously related to AMD and four genes related to AMD in previous studies (SCARB1, ABCA1, APOE, and ALDH3A2) were associated independently with AMD, after adjusting for age and ancestry.]. 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:24346170; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP218417.RAVLAs5_EDDHw5vMuBfCsYTsbUukVVZsxpK4sIsIZKI5I130_publicationInfo { this: dcterms:created "2015-08-25T14:39:44+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }