@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY> .
@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:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_head {
  this: np:hasAssertion dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_assertion;
    np:hasProvenance dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_provenance;
    np:hasPublicationInfo dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_assertion a np:Assertion .
  
  dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_provenance a np:Provenance .
  
  dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_assertion {
  miriam-gene:3792 a ncit:C16612 .
  
  lld:C0398568 a ncit:C7057 .
  
  dgn-gda:DGNe96672c568e0a42c7069b13854b14a8c sio:SIO_000628 miriam-gene:3792, lld:C0398568;
    a sio:SIO_001121 .
}

dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_provenance {
  dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_assertion dcterms:description
      "[The latest postulated diagnoses for Henry are the coexistence of both Kell blood group antigenicity (possibly inherited from Jacquetta Woodville, Henry's maternal great grandmother) causing related impaired fertility, and McLeod syndrome, causing psychotic changes.]. 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:24350322;
    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:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:22+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" .
}