@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ> .
@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:NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ130_head {
   this: np:hasAssertion dgn-np:NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ130_assertion ;
    np:hasProvenance dgn-np:NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ130_assertion a np:Assertion .
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  dgn-np:NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ130_assertion {
   miriam-gene:1406 a ncit:C16612 .
  lld:C0339525 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ130_provenance {
   dgn-np:NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ130_assertion dcterms:description "[To devise an effective method for detecting mutations in 12 genes (CA4, CRX, IMPDH1, NR2E3, RP9, PRPF3, PRPF8, PRPF31, PRPH2, RHO, RP1, and TOPORS) commonly associated with autosomal dominant retinitis pigmentosa (adRP) that account for more than 95% of known mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP197664.RAlSuzER0XiW86ay5TSUOqAUDjxRuzCfza6zEbvbkHrzQ130_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 ;
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    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> ;
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}