@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:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_head { this: np:hasAssertion dgn-np:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_assertion; np:hasProvenance dgn-np:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_provenance; np:hasPublicationInfo dgn-np:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_publicationInfo; a np:Nanopublication . dgn-np:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_assertion a np:Assertion . dgn-np:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_provenance a np:Provenance . dgn-np:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_publicationInfo a np:PublicationInfo . } dgn-np:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_assertion { miriam-gene:2130 a ncit:C16612 . lld:C3536893 a ncit:C7057 . dgn-gda:DGN04d52f1acbd7f52bf87138f7a63951e6 sio:SIO_000628 miriam-gene:2130, lld:C3536893; a sio:SIO_001121 . } dgn-np:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_provenance { dgn-np:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_assertion dcterms:description "[As a result, it was not until the discovery that these tumors share a common underlying molecular pathogenesis (chromosomal translocations involving the EWS gene and one of several members of the ETS family of transcription factors) that significant advances in the diagnosis and therapy of ESFT became possible.]. 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:18088234; 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:NP645838.RAgka6Nld5Bs_AUaGDwe2zTELTNmUwCmuO4IACyp1rm28130_publicationInfo { this: dcterms:created "2016-05-13T12:46:38+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" . }