@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:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_head { this: np:hasAssertion dgn-np:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_assertion; np:hasProvenance dgn-np:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_provenance; np:hasPublicationInfo dgn-np:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_publicationInfo; a np:Nanopublication . dgn-np:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_assertion a np:Assertion . dgn-np:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_provenance a np:Provenance . dgn-np:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_publicationInfo a np:PublicationInfo . } dgn-np:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_assertion { miriam-gene:6390 a ncit:C16612 . lld:C0032002 a ncit:C7057 . dgn-gda:DGNa95712b7a06071b64c48e4a9b7c1e264 sio:SIO_000628 miriam-gene:6390, lld:C0032002; a sio:SIO_001122 . } dgn-np:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_provenance { dgn-np:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_assertion dcterms:description "[This editorial summarizes some of these advances: the identification of the AIP, and the PDE11A and PDE8B genes by genome-wide association (GWA) studies as predisposing genes for pituitary and adrenal tumours, respectively, the discovery of p27 mutations in a new form of MEN similar to MEN type 1 (MEN 1) that is now known as MEN 4, the molecular investigations of Carney triad (CT), a disorder that associates paragangliomas (PGLs), gastrointestinal stromal tumour (GISTs), and pulmonary chondromas (PCH) with pheochromocytomas and adrenocortical adenomas and other lesions, and the molecular elucidation of the association of GISTs with paragangliomas (Carney-Stratakis syndrome) that is now known to be because of SDHB, SDHC, and SDHD mutations.]. 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:19522821; 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:NP745023.RAqdr9BUF7uB1hdtTKNDewJnP6b9iR66NdlI3XCQJJsGY130_publicationInfo { this: dcterms:created "2016-05-13T12:47:23+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" . }