@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:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_head { this: np:hasAssertion dgn-np:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_assertion; np:hasProvenance dgn-np:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_provenance; np:hasPublicationInfo dgn-np:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_publicationInfo; a np:Nanopublication . dgn-np:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_assertion a np:Assertion . dgn-np:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_provenance a np:Provenance . dgn-np:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_publicationInfo a np:PublicationInfo . } dgn-np:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_assertion { miriam-gene:3122 a ncit:C16612 . lld:C0242583 a ncit:C7057 . dgn-gda:DGN5a5849f572f9823e1e33118a0ea2a722 sio:SIO_000628 miriam-gene:3122, lld:C0242583; a sio:SIO_001121 . } dgn-np:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_provenance { dgn-np:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_assertion dcterms:description "[Using an in vitro transcription system based on the HLA-DRA promoter, we show here that extracts from RFX-deficient cells from patients with BLS (BLS cells) in groups B and C, which are transcriptionally inactive in this assay, can be complemented to full transcriptional activity by the purified RFX.]. 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:7935401; 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:NP1327515.RAGbzrl4ynQjXTPqo3ymxZ1ZnLfNypj6r0CphlLHjCDDs130_publicationInfo { this: dcterms:created "2016-05-13T12:51:48+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" . }