@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:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_head { this: np:hasAssertion dgn-np:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_assertion; np:hasProvenance dgn-np:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_provenance; np:hasPublicationInfo dgn-np:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_publicationInfo; a np:Nanopublication . dgn-np:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_assertion a np:Assertion . dgn-np:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_provenance a np:Provenance . dgn-np:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_publicationInfo a np:PublicationInfo . } dgn-np:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_assertion { miriam-gene:668 a ncit:C16612 . lld:C1862261 a ncit:C7057 . dgn-gda:DGNb275a7701b099d7a3c787bf3bc00e8f5 sio:SIO_000628 miriam-gene:668, lld:C1862261; a sio:SIO_001121 . } dgn-np:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_provenance { dgn-np:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_assertion dcterms:description "[MDR analysis for intragenic mutations of FOXL2 gene reported in previous BPES studies indicated that the mutations which led to much stronger disturbance of amino acid sequence were responsible for more type I BPES, while other kinds of mutation were responsible for more type II BPES.]. 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:19592504; 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:NP270476.RApAljtCyKRZewavsy6Wbvd-2DjZTUeXS59_iufaAsU8s130_publicationInfo { this: dcterms:created "2015-08-25T14:40:14+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" . }