@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc> .
@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:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_head {
  this: np:hasAssertion dgn-np:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_assertion;
    np:hasProvenance dgn-np:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_provenance;
    np:hasPublicationInfo dgn-np:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_assertion a np:Assertion .
  
  dgn-np:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_provenance a np:Provenance .
  
  dgn-np:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_assertion {
  miriam-gene:6520 a ncit:C16612 .
  
  lld:C0019069 a ncit:C7057 .
  
  dgn-gda:DGN2c2f5db954f57b804253ca114e2ebe3e sio:SIO_000628 miriam-gene:6520, lld:C0019069;
    a sio:SIO_001121 .
}

dgn-np:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_provenance {
  dgn-np:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_assertion dcterms:description
      "[Mutations known to cause hemophilia Bm occur at residue 180, 181, or 182 near the amino terminus of the heavy chain and at residue 311, 364, 368, 390, 396, or 397 near the activation site of factor IX (Giannelli et al., 1990).]. 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:8518277;
    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:NP696548.RACsxJ5URTNNfPvHpMYQsK3lV035eV6Y7ybgIii12s0jc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:40+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" .
}