@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:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_head { this: np:hasAssertion dgn-np:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_assertion; np:hasProvenance dgn-np:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_provenance; np:hasPublicationInfo dgn-np:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_publicationInfo; a np:Nanopublication . dgn-np:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_assertion a np:Assertion . dgn-np:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_provenance a np:Provenance . dgn-np:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_publicationInfo a np:PublicationInfo . } dgn-np:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_assertion { miriam-gene:4653 a ncit:C16612 . lld:C0339573 a ncit:C7057 . dgn-gda:DGNf29493d26aacb20b5d70a386bf46657a sio:SIO_000628 miriam-gene:4653, lld:C0339573; a sio:SIO_001121 . } dgn-np:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_provenance { dgn-np:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_assertion dcterms:description "[Although TIGR/myocilin and optineurin mutations have been shown to be causally linked to POAG in other populations, findings from this study do not support either of these as causative genes in an Afro-Caribbean population known to have relatively high rates of POAG.]. 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:12616399; 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:NP385612.RAK49iW0G2tBfwD_aLiY8QrSOepWvZ_W3s0S2p_qGLm9E130_publicationInfo { this: dcterms:created "2016-05-13T12:44:40+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" . }