@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I> .
@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/v3.0.0/void/> .

dgn-np:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_head {
  this: np:hasAssertion dgn-np:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_assertion;
    np:hasProvenance dgn-np:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_provenance;
    np:hasPublicationInfo dgn-np:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_assertion a np:Assertion .
  
  dgn-np:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_provenance a np:Provenance .
  
  dgn-np:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_assertion {
  miriam-gene:1351 a ncit:C16612 .
  
  lld:C0019069 a ncit:C7057 .
  
  dgn-gda:DGN87c28c4878e73f99ea02cd46312338ff sio:SIO_000628 miriam-gene:1351, lld:C0019069;
    a sio:SIO_001121 .
}

dgn-np:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_provenance {
  dgn-np:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_assertion dcterms:description
      "[The F8 of a patient with mild congenital haemophilia A, in whom no candidate mutation was found in the exons or their flanking regions, was analysed in detail to identify the patient's aetiological genetic abnormality.]. 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:22776136;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP322911.RAeKBkPElUIJFnW2jtPqNp-MdmnU8lByRbMVeJtzN_-8I130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:45+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}