@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:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_head { this: np:hasAssertion dgn-np:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_assertion; np:hasProvenance dgn-np:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_provenance; np:hasPublicationInfo dgn-np:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_publicationInfo; a np:Nanopublication . dgn-np:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_assertion a np:Assertion . dgn-np:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_provenance a np:Provenance . dgn-np:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_publicationInfo a np:PublicationInfo . } dgn-np:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_assertion { miriam-gene:668 a ncit:C16612 . lld:C0025322 a ncit:C7057 . dgn-gda:DGNb1eb3f1d8cf7c93d3e291c939533639b sio:SIO_000628 miriam-gene:668, lld:C0025322; a sio:SIO_001121 . } dgn-np:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_provenance { dgn-np:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_assertion dcterms:description "[FOXL2 is a transcription factor that is essential for ovarian function and maintenance, the germline mutations of which give rise to the blepharophimosis ptosis epicanthus inversus syndrome (BPES), often associated with premature ovarian failure.]. 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:24817949; 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:NP1181558.RAqpIml3tKQxep2c8guNNxSshg0pswj0id_FfOUjkwq54130_publicationInfo { this: dcterms:created "2016-05-13T12:50:41+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" . }