@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:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_head { this: np:hasAssertion dgn-np:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_assertion; np:hasProvenance dgn-np:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_provenance; np:hasPublicationInfo dgn-np:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_publicationInfo; a np:Nanopublication . dgn-np:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_assertion a np:Assertion . dgn-np:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_provenance a np:Provenance . dgn-np:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_publicationInfo a np:PublicationInfo . } dgn-np:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_assertion { miriam-gene:2332 a ncit:C16612 . lld:C0016667 a ncit:C7057 . dgn-gda:DGNaa6b292de1dee61cb90a93403d6878f9 sio:SIO_000628 miriam-gene:2332, lld:C0016667; a sio:SIO_001121 . } dgn-np:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_provenance { dgn-np:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_assertion dcterms:description "[This preliminary study suggests that regionally specific alterations of white matter integrity occur in females with fragile X. Aberrant white matter connectivity in these regions is consistent with the profile of cognitive and behavioral features of fragile X syndrome, and potentially provide additional insight into the detrimental effects of suboptimal levels of FMRP in the developing brain.]. 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:12627472; 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:NP386357.RAgDy3B-rOyrDgKXns41DSsndH2LJX6DsuJh2ZYoaOgw4130_publicationInfo { this: dcterms:created "2016-05-13T12:44:40+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" . }