@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM> .
@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:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_head {
  this: np:hasAssertion dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_assertion;
    np:hasProvenance dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_provenance;
    np:hasPublicationInfo dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_assertion a np:Assertion .
  
  dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_provenance a np:Provenance .
  
  dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_assertion {
  miriam-gene:5660 a ncit:C16612 .
  
  lld:C0085650 a ncit:C7057 .
  
  dgn-gda:DGN3505e7b93ed791ecb8b29ba368ab1f87 sio:SIO_000628 miriam-gene:5660, lld:C0085650;
    a sio:SIO_001121 .
}

dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_provenance {
  dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_assertion dcterms:description
      "[Although the homozygous deficiency of protein C has been reported to be closely associated with fatal purpura fulminans or severe and massive thrombotic diseases during the neonatal period, the patient had survived the neonatal period without any clinical manifestations relevant to thrombosis.]. 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:3840289;
    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:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:08+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" .
}