@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1124438.RAn8knt5n_Ux549OzGfaIn0SEkwbQmRGf4nknijmLjLCQ> .
@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:NP1124438.RAn8knt5n_Ux549OzGfaIn0SEkwbQmRGf4nknijmLjLCQ130_head {
  this: np:hasAssertion dgn-np:NP1124438.RAn8knt5n_Ux549OzGfaIn0SEkwbQmRGf4nknijmLjLCQ130_assertion ;
    np:hasProvenance dgn-np:NP1124438.RAn8knt5n_Ux549OzGfaIn0SEkwbQmRGf4nknijmLjLCQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP1124438.RAn8knt5n_Ux549OzGfaIn0SEkwbQmRGf4nknijmLjLCQ130_publicationInfo ;
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dgn-np:NP1124438.RAn8knt5n_Ux549OzGfaIn0SEkwbQmRGf4nknijmLjLCQ130_assertion {
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dgn-np:NP1124438.RAn8knt5n_Ux549OzGfaIn0SEkwbQmRGf4nknijmLjLCQ130_provenance {
  dgn-np:NP1124438.RAn8knt5n_Ux549OzGfaIn0SEkwbQmRGf4nknijmLjLCQ130_assertion dcterms:description "[Genome-wide gene expression profiling by MACE (Massive Analysis of cDNA Ends) identified 80 genes to be differentially expressed between HD patients and controls, which could be linked to cardiovascular disease (e.g., KLF6, DUSP6, KLF4), to infection / immune disease (e.g., ZFP36, SOCS3, JUND), and to distinct proatherogenic pathways such as the Toll-like receptor signaling pathway (e.g., IL1B, MYD88, TICAM2), the MAPK signaling pathway (e.g., DUSP1, FOS, HSPA1A), and the chemokine signaling pathway (e.g., RHOA, PAK1, CXCL5).]. 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:NP1124438.RAn8knt5n_Ux549OzGfaIn0SEkwbQmRGf4nknijmLjLCQ130_publicationInfo {
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