@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0> .
@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#> .
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  this: np:hasAssertion dgn-np:NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0130_assertion ;
    np:hasProvenance dgn-np:NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0130_provenance ;
    np:hasPublicationInfo dgn-np:NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0130_assertion a np:Assertion .
  dgn-np:NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0130_provenance a np:Provenance .
  dgn-np:NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0130_assertion {
  miriam-gene:6519 a ncit:C16612 .
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dgn-np:NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0130_provenance {
  dgn-np:NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0130_assertion dcterms:description "[In conclusion, we developed a reliable and robust MLPA analytic method for SLC3A1 and SLC7A9 genes that represents an optimal complement to DNA sequence analysis in patients with cystinuria, enabling the screening for deletions and duplications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP61992.RAkQHK-hJhnFTwyFA93Qi052gc9JqY1k2rIXHZz9DRF_0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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