@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg> .
@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:NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg130_head {
  this: np:hasAssertion dgn-np:NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg130_assertion;
    np:hasProvenance dgn-np:NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg130_provenance;
    np:hasPublicationInfo dgn-np:NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg130_provenance a np:Provenance .
  
  dgn-np:NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg130_assertion {
  miriam-gene:7124 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg130_provenance {
  dgn-np:NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg130_assertion dcterms:description
      "[We now describe data on the association between TNF microsatellite polymorphisms, first on susceptibility in 202 controls and 133 cases each having two to 30 BCCs, and secondly, within the cases, on BCC numbers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP477306.RAAWQR2_j2PbIT3KvxHlkDZGYwWTueZ_nDplbBnqACsYg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:46+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;
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