@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI> .
@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:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_head {
  this: np:hasAssertion dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_assertion ;
    np:hasProvenance dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_provenance ;
    np:hasPublicationInfo dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_assertion a np:Assertion .
  dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_provenance a np:Provenance .
  dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_assertion {
  miriam-gene:3047 a ncit:C16612 .
  lld:C1868112 a ncit:C7057 .
  dgn-gda:DGNd8c307541e8a51ade9e772d93132610c sio:SIO_000628 miriam-gene:3047 , lld:C1868112 ;
    a sio:SIO_001121 .
}
dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_provenance {
  dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_assertion dcterms:description "[Using gel retardation assays on various nuclear extracts, we also demonstrated that this novel mutation abolishes the binding of the ubiquitous CCAAT binding factor, CP1 to the distal CCAAT motif of the gamma-globin gene but does not affect the binding of any erythroid specific factor, thereby suggesting a possible role for CP1 in the developmental regulation of fetal globin expression.]. 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:1698280 ;
    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:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:28+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" .
}