@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw> .
@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:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_head {
  this: np:hasAssertion dgn-np:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_assertion;
    np:hasProvenance dgn-np:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_provenance;
    np:hasPublicationInfo dgn-np:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_assertion a np:Assertion .
  
  dgn-np:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_provenance a np:Provenance .
  
  dgn-np:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_assertion {
  miriam-gene:4068 a ncit:C16612 .
  
  lld:C0009447 a ncit:C7057 .
  
  dgn-gda:DGNf924cb5257efa1a1dba67b4db5bdf1b1 sio:SIO_000628 miriam-gene:4068, lld:C0009447;
    a sio:SIO_001121 .
}

dgn-np:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_provenance {
  dgn-np:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_assertion dcterms:description
      "[We therefore suggest that XLP should be suspected in certain boys previously diagnosed as having CVID and recommend that patients are investigated both by genetic analysis of SH2D1A and by expression of SAP protein.]. 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:10898506;
    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:NP620799.RAIV7B9s3N4T0x_aonx5NKbBs1lLi_kH82OgU6o6Expcw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:15+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" .
}