@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8> .
@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:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_head {
  this: np:hasAssertion dgn-np:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_assertion;
    np:hasProvenance dgn-np:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_provenance;
    np:hasPublicationInfo dgn-np:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_assertion a np:Assertion .
  
  dgn-np:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_provenance a np:Provenance .
  
  dgn-np:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_assertion {
  miriam-gene:7538 a ncit:C16612 .
  
  lld:C1268935 a ncit:C7057 .
  
  dgn-gda:DGNc8bf024ce23f7c065dcb18d9dc37c132 sio:SIO_000628 miriam-gene:7538, lld:C1268935;
    a sio:SIO_001121 .
}

dgn-np:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_provenance {
  dgn-np:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_assertion dcterms:description
      "[The quantification of residual plasmatic ADAMTS13 activity in congenital thrombotic thrombocytopenic purpura (TTP) patients is constrained by limitations in sensitivity and reproducibility of commonly used assays at low levels of ADAMTS13 activity, blunting efforts to establish genotype-phenotype correlations.]. 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:22529288;
    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:NP426301.RAh7Oo5ICIUUQg79snx3LfC1d41S5hes3d4TN7jinrfU8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:13+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" .
}