@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo130_head {
   this: np:hasAssertion dgn-np:NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo130_assertion ;
    np:hasProvenance dgn-np:NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo130_provenance ;
    np:hasPublicationInfo dgn-np:NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo130_publicationInfo ;
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  dgn-np:NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo130_provenance a np:Provenance .
  dgn-np:NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo130_assertion {
   miriam-gene:114327 a ncit:C16612 .
  lld:C0270853 a ncit:C7057 .
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dgn-np:NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo130_provenance {
   dgn-np:NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo130_assertion dcterms:description "[Here, we describe detailed physical and transcriptome maps of the 3.5cM EJM1 region, and detailed results of mutation analyses for the remained 14 genes (HELO1, GCMA, KIAA0936, FBXO9, GSTA3, GSTA4, PTD011, KIAA0576, LMPB1, IL17F, MCM3, PKHD1, KIAA0105, TFAP2B) in patients with JME.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP561928.RAXtZvLjZRpOusgRAAeSe7cj3_OdhoHDp8dnqq0wQreFo130_publicationInfo {
   this: dcterms:created "2016-05-13T12:45:59+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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}