@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA> .
@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:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_head {
  this: np:hasAssertion dgn-np:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_assertion ;
    np:hasProvenance dgn-np:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_provenance ;
    np:hasPublicationInfo dgn-np:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_assertion a np:Assertion .
  dgn-np:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_provenance a np:Provenance .
  dgn-np:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_assertion {
  miriam-gene:4942 a ncit:C16612 .
  lld:C0339528 a ncit:C7057 .
  dgn-gda:DGN8ce19ebd82f126384b096d2192025128 sio:SIO_000628 miriam-gene:4942 , lld:C0339528 ;
    a sio:SIO_001121 .
}
dgn-np:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_provenance {
  dgn-np:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_assertion dcterms:description "[A restriction fragment length polymorphism (RFLP) was identified in the functional OAT gene sequence with EcoRI which may be useful for prenatal diagnosis of GA. RFLPs were also identified in the OAT-related gene sequences located on the X chromosome with Hind III and Pst I which may potentially show linkage to X-linked retinitis pigmentosa locus.]. 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:3417397 ;
    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:NP198433.RAiGPWpZ07fHZQei3qxxaQFLb7mdT3C5Ex55c3NXBcsgA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:49+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" .
}