@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw> .
@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:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_head {
   this: np:hasAssertion dgn-np:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_assertion ;
    np:hasProvenance dgn-np:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_provenance ;
    np:hasPublicationInfo dgn-np:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_assertion a np:Assertion .
  dgn-np:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_provenance a np:Provenance .
  dgn-np:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_assertion {
   miriam-gene:5538 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
  dgn-gda:DGNe6ea0b2b6a71a5e4bd23c92fc4d93a23 sio:SIO_000628 miriam-gene:5538 , lld:C0007097 ;
    a sio:SIO_001121 .
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dgn-np:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_provenance {
   dgn-np:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_assertion dcterms:description "[We have examined mRNA levels of the CLN1, CLN2, and CLN3 genes, which are associated with the infantile, late infantile, and juvenile forms of NCL in 64 different human tissues, and have grouped the results into gastrointestinal tract, central nervous system, glandular/secretory, muscle, and carcinoma tissue types.]. 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:NP290675.RAsr10d17zyQCCblanIoRCEGSKYla7kxKtayE_XIQ3Zuw130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:45+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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