@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM> .
@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:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_head {
  this: np:hasAssertion dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_assertion;
    np:hasProvenance dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_provenance;
    np:hasPublicationInfo dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_assertion a np:Assertion .
  
  dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_provenance a np:Provenance .
  
  dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_assertion {
  miriam-gene:4153 a ncit:C16612 .
  
  lld:C0035436 a ncit:C7057 .
  
  dgn-gda:DGNfef31294af0ebcd2b5a15cafd2f69538 sio:SIO_000628 miriam-gene:4153, lld:C0035436;
    a sio:SIO_001121 .
}

dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_provenance {
  dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_assertion dcterms:description
      "[As high levels of MBL and MBL2 associated genotypes have previously been seen to be associated with CRHD, we investigated the association between MBL2 polymorphisms and the presence of acute carditis and arthritis in patients with a history of RF.]. 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:18602696;
    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:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:58+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" .
}