@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0> .
@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:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_head {
  this: np:hasAssertion dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_assertion ;
    np:hasProvenance dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_provenance ;
    np:hasPublicationInfo dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_assertion {
  miriam-gene:7305 a ncit:C16612 .
  lld:C0011303 a ncit:C7057 .
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dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_provenance {
  dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_assertion dcterms:description "[The genes of the DAP12-TREM2 signaling receptor are located on 19q13.12 and 6p21.1, to which linkage has been observed also in families affected by another immune-mediated demyelinating disease, MS. We have tested if allelic variation in DAP12 or TREM2 predisposes also to MS by monitoring carrier frequency of the Finnish PLOSL mutation in Finnish MS cases and by studying DAP12 and TREM2 in MS by linkage and association.]. 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:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:23+02:00"^^xsd:dateTime ;
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