@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME> .
@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:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_head {
   this: np:hasAssertion dgn-np:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_assertion ;
    np:hasProvenance dgn-np:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_provenance ;
    np:hasPublicationInfo dgn-np:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_assertion a np:Assertion .
  dgn-np:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_provenance a np:Provenance .
  dgn-np:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_assertion {
   miriam-gene:90226 a ncit:C16612 .
  lld:C0085655 a ncit:C7057 .
  dgn-gda:DGNa20a1b0659b8c5521bd98fd6003523c3 sio:SIO_000628 miriam-gene:90226 , lld:C0085655 ;
    a sio:SIO_001121 .
}
dgn-np:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_provenance {
   dgn-np:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_assertion dcterms:description "[The anti-SRP group, which had exclusively juvenile polymyositis, was characterized by high frequencies of black race, severe onset, distal weakness, falling episodes, Raynaud phenomenon, cardiac involvement, high CK levels, chronic disease course, frequent hospitalization, and wheelchair use.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:23877355 ;
    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:NP379576.RALvMn7jGDtaXzEWFHkZ2XQ0shA_cAIb7c_2Msl4mdmME130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:44+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}