@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM> .
@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:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_head {
  this: np:hasAssertion dgn-np:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_assertion ;
    np:hasProvenance dgn-np:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_provenance ;
    np:hasPublicationInfo dgn-np:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_assertion a np:Assertion .
  dgn-np:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_provenance a np:Provenance .
  dgn-np:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_assertion {
  miriam-gene:5710 a ncit:C16612 .
  lld:C0270814 a ncit:C7057 .
  dgn-gda:DGN639b23471b1ec7800edb89404d4fec5b sio:SIO_000628 miriam-gene:5710 , lld:C0270814 ;
    a sio:SIO_001121 .
}
dgn-np:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_provenance {
  dgn-np:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_assertion dcterms:description "[The use of previously established sequence matrices for the scoring of putative ESE motifs showed that the adjacent silent and missense mutations are located within highly conserved overlapping stretches of seven nucleotides with a close similarity to the ESE-specific consensus sequences recognised by the SC35 and SF2/ASF SR proteins.]. 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:13680360 ;
    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:NP483731.RAp-kTX6t8O-RApFp6-Iiqqnb43Yka-aEEWhF9UmDneZM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:49+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" .
}