@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:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_head { this: np:hasAssertion dgn-np:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_assertion; np:hasProvenance dgn-np:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_provenance; np:hasPublicationInfo dgn-np:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_publicationInfo; a np:Nanopublication . dgn-np:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_assertion a np:Assertion . dgn-np:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_provenance a np:Provenance . dgn-np:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_publicationInfo a np:PublicationInfo . } dgn-np:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_assertion { miriam-gene:10743 a ncit:C16612 . lld:C0795864 a ncit:C7057 . dgn-gda:DGNbcdf81dcc12130015f45e52001b66b17 sio:SIO_000628 miriam-gene:10743, lld:C0795864; a sio:SIO_001121 . } dgn-np:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_provenance { dgn-np:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_assertion dcterms:description "[Our results show that Rai1 dosage has major consequences on molecular processes involved in growth, development, and neurological and behavioral functions, thus providing evidence for several dosage-thresholds for phenotypic manifestations causing dup(17)(p11.2) syndrome or SMS in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_curated; sio:SIO_000772 miriam-pubmed:18285828; prov:wasDerivedFrom dgn-void:ctd_human-20150221; prov:wasGeneratedBy eco:ECO_0000218 . dgn-void:ctd_human-20150221 pav:importedOn "2015-02-21"^^xsd:date . dgn-void:source_evidence_curated a eco:ECO_0000205; rdfs:comment "Gene-disease associations manually curated."@en; rdfs:label "DisGeNET evidence - CURATED"@en . } dgn-np:NP28148.RANB7Mlq6yhpuR99Lz_pnpFlpXDUZdClJSLGN1dgJDOeI130_publicationInfo { this: dcterms:created "2015-08-25T14:37:56+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" . }