@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M> .
@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:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_head {
  this: np:hasAssertion dgn-np:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_assertion;
    np:hasProvenance dgn-np:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_provenance;
    np:hasPublicationInfo dgn-np:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_assertion a np:Assertion .
  
  dgn-np:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_provenance a np:Provenance .
  
  dgn-np:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_assertion {
  miriam-gene:7504 a ncit:C16612 .
  
  lld:C0000744 a ncit:C7057 .
  
  dgn-gda:DGN2bb949a61b8f31c8d1a590ce82f48623 sio:SIO_000628 miriam-gene:7504, lld:C0000744;
    a sio:SIO_001121 .
}

dgn-np:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_provenance {
  dgn-np:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_assertion dcterms:description
      "[The McLeod phenotype is derived from various forms of XK gene defects that result in the absence of XK protein, and is defined hematologically by the absence of Kx antigen, weakening of Kell system antigens, and red cell acanthocytosis.]. 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:17300882;
    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:NP277274.RA0JSKckZhOGx1aIJ-HSQRh9z7NRH1fQcxee-eDp7SC2M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:36+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" .
}