@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss> .
@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:NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss130_head {
  this: np:hasAssertion dgn-np:NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss130_assertion ;
    np:hasProvenance dgn-np:NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss130_provenance ;
    np:hasPublicationInfo dgn-np:NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss130_provenance a np:Provenance .
  dgn-np:NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss130_assertion {
  miriam-gene:5008 a ncit:C16612 .
  lld:C0033774 a ncit:C7057 .
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dgn-np:NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss130_provenance {
  dgn-np:NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss130_assertion dcterms:description "[OSM and IL-31 signaling have been implicated in keratinocyte cell proliferation, differentiation, apoptosis, and inflammation, but our OSMR data in individuals with FPLCA represent the first human germline mutations in this cytokine receptor complex and provide new insight into mechanisms of skin itching.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP822928.RAqUkapdLLenAYjlbsnJuWyt5Uqh6AunIgcoToWo9M2ss130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:24+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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