@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:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_head { this: np:hasAssertion dgn-np:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_assertion; np:hasProvenance dgn-np:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_provenance; np:hasPublicationInfo dgn-np:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_publicationInfo; a np:Nanopublication . dgn-np:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_assertion a np:Assertion . dgn-np:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_provenance a np:Provenance . dgn-np:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_publicationInfo a np:PublicationInfo . } dgn-np:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_assertion { miriam-gene:4867 a ncit:C16612 . lld:C0431399 a ncit:C7057 . dgn-gda:DGNb805c7e893ee768651ed0665fba2774f sio:SIO_000628 miriam-gene:4867, lld:C0431399; a sio:SIO_001121 . } dgn-np:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_provenance { dgn-np:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_assertion dcterms:description "[Review of this disorder and related syndromes suggests that (1) hypoplasia of the cerebellar vermis in Joubert syndrome is frequently associated with a complex brain stem malformation represented as the molar tooth sign on magnetic resonance imaging, (2) the molar tooth sign could be present in association with the Dandy-Walker malformation and occipital encephalocele, (3) cerebellar hypoplasia is present in conditions related to Joubert syndrome such as Arima syndrome; Senior-Loken syndrome; cerebellar vermian hypoplasia, oligophrenia, congenital ataxia, coloboma, and hepatic fibrosis syndrome; and juvenile nephronophthisis due to NPH1 mutations, and (4) the brainstem-vermis malformation spectrum is probably caused by at least two and probably several genetic loci.]. 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:10511339; 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:NP264784.RAgluMq56mHZ7ctzj4SMv_xkZ1ZoHDbV094LISZwLB0M4130_publicationInfo { this: dcterms:created "2016-05-13T12:43:46+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" . }