@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:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_head { this: np:hasAssertion dgn-np:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_assertion; np:hasProvenance dgn-np:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_provenance; np:hasPublicationInfo dgn-np:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_publicationInfo; a np:Nanopublication . dgn-np:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_assertion a np:Assertion . dgn-np:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_provenance a np:Provenance . dgn-np:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_publicationInfo a np:PublicationInfo . } dgn-np:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_assertion { miriam-gene:10215 a ncit:C16612 . lld:C0017638 a ncit:C7057 . dgn-gda:DGN6768a4db1bca55ee81f73c77c2cc1c9d sio:SIO_000628 miriam-gene:10215, lld:C0017638; a sio:SIO_001121 . } dgn-np:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_provenance { dgn-np:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_assertion dcterms:description "[In contrast to the various types of pediatric astrocytic tumors, all ependymomas WHO grade II, regardless of site of origin, showed at most minimal OLIG2 expression, suggesting that OLIG2 function in pediatric gliomas is cell lineage dependent.]. 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:21193945; 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:NP862259.RAAmk8GfdJqi-hlZmY697Ep0tmzOSp6ROPacj3SfOO2-4130_publicationInfo { this: dcterms:created "2016-05-13T12:48:15+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" . }