@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_head {
  this: np:hasAssertion dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_assertion;
    np:hasProvenance dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_provenance;
    np:hasPublicationInfo dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_assertion a np:Assertion .
  
  dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_provenance a np:Provenance .
  
  dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_assertion {
  miriam-gene:6948 a ncit:C16612 .
  
  lld:C0017154 a ncit:C7057 .
  
  dgn-gda:DGN0a3d9a4e10b2e273b097f3d73d0120ca sio:SIO_000628 miriam-gene:6948, lld:C0017154;
    a sio:SIO_001122 .
}

dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_provenance {
  dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_assertion dcterms:description
      "[A genetic variant of TCN2 (rs9606756) related to lower vitamin B12 levels was more frequent in pernicious anaemia patients compared to controls, showing the plausibility of genetic factors determining the possible clinical manifestation of autoimmune gastritis.]. 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:25681243;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:19+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}