@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms> .
@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:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_head {
  this: np:hasAssertion dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_assertion;
    np:hasProvenance dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_provenance;
    np:hasPublicationInfo dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_assertion a np:Assertion .
  
  dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_provenance a np:Provenance .
  
  dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_assertion {
  miriam-gene:5554 a ncit:C16612 .
  
  lld:C0008533 a ncit:C7057 .
  
  dgn-gda:DGNbbf11fc638d2f80d82cd31bf72d2c2ba sio:SIO_000628 miriam-gene:5554, lld:C0008533;
    a sio:SIO_001121 .
}

dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_provenance {
  dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_assertion dcterms:description
      "[The likelihood of a missense mutation causing hemophilia B depends on whether the residue is also conserved in the factor IX-related proteases: factor VII, factor X, and protein C. Most of the possible missense mutations in generically conserved residues (i.e., those conserved in factor IX and in all the related proteases) should cause disease.]. 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:1680287;
    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:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:36+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" .
}