@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE> .
@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:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_head {
  this: np:hasAssertion dgn-np:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_assertion;
    np:hasProvenance dgn-np:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_provenance;
    np:hasPublicationInfo dgn-np:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_assertion a np:Assertion .
  
  dgn-np:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_provenance a np:Provenance .
  
  dgn-np:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_assertion {
  miriam-gene:2158 a ncit:C16612 .
  
  lld:C0008533 a ncit:C7057 .
  
  dgn-gda:DGNd0643e269debbf1b50a3ef6e9deba4a0 sio:SIO_000628 miriam-gene:2158, lld:C0008533;
    a sio:SIO_001121 .
}

dgn-np:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_provenance {
  dgn-np:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_assertion dcterms:description
      "[Hemophilia B is a useful model for studying the underlying pattern of recent germline mutations in humans because the observed pattern of mutation in factor IX more closely reflects the underlying pattern of mutation than the observed pattern for many other genes.]. 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:1634040;
    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:NP526275.RA0LcENdDi-jjqgHbHHRP2Ds2RTD0UIC-kkTu8Xzh9QPE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:43+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" .
}