@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:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_head { this: np:hasAssertion dgn-np:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_assertion; np:hasProvenance dgn-np:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_provenance; np:hasPublicationInfo dgn-np:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_publicationInfo; a np:Nanopublication . dgn-np:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_assertion a np:Assertion . dgn-np:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_provenance a np:Provenance . dgn-np:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_publicationInfo a np:PublicationInfo . } dgn-np:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_assertion { miriam-gene:6281 a ncit:C16612 . lld:C0025149 a ncit:C7057 . dgn-gda:DGN439f1e0709875ed35b238e1c06fad9a4 sio:SIO_000628 miriam-gene:6281, lld:C0025149; a sio:SIO_001121 . } dgn-np:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_provenance { dgn-np:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_assertion dcterms:description "[Assessed against these normal tissue-specific methylation states, S100A6 and S100A10 demonstrated tumour-specific hypermethylation in medulloblastoma primary tumours (5 out of 40 and 4 out of 35, respectively, both 12%) and cell lines (both 7 out of 9, 78%), which was associated with their transcriptional silencing.]. 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:17579622; 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:NP28953.RAjlnMPojsVn1k8flli53pSrOhR-8wqdgxggyTljlFJAA130_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" . }