@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw> .
@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:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_head {
  this: np:hasAssertion dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_assertion ;
    np:hasProvenance dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_provenance ;
    np:hasPublicationInfo dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_assertion a np:Assertion .
  dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_provenance a np:Provenance .
  dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_assertion {
  miriam-gene:4810 a ncit:C16612 .
  lld:C0424605 a ncit:C7057 .
  dgn-gda:DGN86bc93acaa9b840063455f8f2041d8e3 sio:SIO_000628 miriam-gene:4810 , lld:C0424605 ;
    a sio:SIO_001121 .
}
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_provenance {
  dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_assertion dcterms:description "[Audit of findings from application of array CGH for patients referred for developmental delay, behavioural abnormalities and birth defects in 4805 patients referred to Guy's and St Thomas' NHS Foundation Trust for cytogenetic investigation from South East London, Kent and East Sussex and other genetic centres across the UK.]. 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:21429933 ;
    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:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:59+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" .
}