@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA> .
@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:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_head {
  this: np:hasAssertion dgn-np:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_assertion;
    np:hasProvenance dgn-np:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_provenance;
    np:hasPublicationInfo dgn-np:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_assertion a np:Assertion .
  
  dgn-np:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_provenance a np:Provenance .
  
  dgn-np:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_assertion {
  miriam-gene:26039 a ncit:C16612 .
  
  lld:C0011644 a ncit:C7057 .
  
  dgn-gda:DGN5730dfa44ada01a2a394e6e4a1e39b4c sio:SIO_000628 miriam-gene:26039, lld:C0011644;
    a sio:SIO_001121 .
}

dgn-np:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_provenance {
  dgn-np:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_assertion dcterms:description
      "[More than 100 sera from patients with scleroderma CREST (calcinosis, Raynaud phenomenon, esophageal dismotility, sclerodactyly, telangiectasia) were tested in order to detect antigenic nuclear components of the field bean Vicia faba (2n = 12).]. 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:7704412;
    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:NP181705.RAs-qYqZmWGqrpmGX1ntGUkP-pl0o0xX-n_rlLtGfJ7cA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}