@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:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_head { this: np:hasAssertion dgn-np:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_assertion; np:hasProvenance dgn-np:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_provenance; np:hasPublicationInfo dgn-np:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_publicationInfo; a np:Nanopublication . dgn-np:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_assertion a np:Assertion . dgn-np:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_provenance a np:Provenance . dgn-np:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_publicationInfo a np:PublicationInfo . } dgn-np:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_assertion { miriam-gene:5308 a ncit:C16612 . lld:C3495488 a ncit:C7057 . dgn-gda:DGNb455b32615048305f56ec8126fa195f7 sio:SIO_000628 miriam-gene:5308, lld:C3495488; a sio:SIO_001121 . } dgn-np:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_provenance { dgn-np:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_assertion dcterms:description "[In this work, we have investigated the functional properties of three PITX2 mutants reported in Axenfeld-Rieger syndrome patients relative to the regulation of these genes, using reporter genes under the control of human PRL (hPRL), hGH, or POU1F1 promoters transfected in nonpituitary and pituitary cell lines.]. 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:20978111; 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:NP626516.RA2RxxNgAjxjQn4UFavnw2NSzqpmzbIqUJjiK-tWKg8fA130_publicationInfo { this: dcterms:created "2015-08-25T14:43:55+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" . }