@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_head {
  this: np:hasAssertion dgn-np:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_assertion ;
    np:hasProvenance dgn-np:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_provenance ;
    np:hasPublicationInfo dgn-np:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_assertion a np:Assertion .
  dgn-np:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_provenance a np:Provenance .
  dgn-np:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_assertion {
  miriam-gene:6500 a ncit:C16612 .
  lld:C0009207 a ncit:C7057 .
  dgn-gda:DGN130f544693ea30a464fd34577a56e79c sio:SIO_000628 miriam-gene:6500 , lld:C0009207 ;
    a sio:SIO_001121 .
}
dgn-np:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_provenance {
  dgn-np:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_assertion dcterms:description "[Among these candidate general elongation factors are the positive transcription elongation factor b (P-TEFb), eleven-nineteen lysine-rich in leukemia (ELL), Cockayne syndrome complementation group B (CSB), and elongin proteins, which all function in vitro to expedite elongation by RNA polymerase II by suppressing transient pausing or premature arrest by polymerase through direct interactions with the elongation complex.]. 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:10872452 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP623967.RART8KpVZlmV6klQSJlKcjKCGbNX4K4w84_T47Qelzqhc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:16+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}