@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:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_head { this: np:hasAssertion dgn-np:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_assertion; np:hasProvenance dgn-np:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_provenance; np:hasPublicationInfo dgn-np:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_publicationInfo; a np:Nanopublication . dgn-np:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_assertion a np:Assertion . dgn-np:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_provenance a np:Provenance . dgn-np:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_publicationInfo a np:PublicationInfo . } dgn-np:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_assertion { miriam-gene:2332 a ncit:C16612 . lld:C0025362 a ncit:C7057 . dgn-gda:DGN9506543fa9e266ee42b88b54f18e2dd2 sio:SIO_000628 miriam-gene:2332, lld:C0025362; a sio:SIO_001121 . } dgn-np:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_provenance { dgn-np:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_assertion dcterms:description "[In contrast, a relationship between the second main group of fragile sites characterized by repeat expansion, the rare fragile sites, and mental retardation has been proposed many years ago, but after the molecular cloning of FRAXA and FRAXE both unequivocally involved in mental retardation, no additional fragile sites linked with mental retardation have been cloned for over a decade.]. 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:17567780; 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:NP615047.RAfnS4jAqvPoVDF1_iem7vuqFECNchVYkzCv8N7BKf6jk130_publicationInfo { this: dcterms:created "2016-05-13T12:46:24+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" . }