@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc> .
@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:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_head {
  this: np:hasAssertion dgn-np:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_assertion;
    np:hasProvenance dgn-np:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_provenance;
    np:hasPublicationInfo dgn-np:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_assertion a np:Assertion .
  
  dgn-np:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_provenance a np:Provenance .
  
  dgn-np:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_assertion {
  miriam-gene:81618 a ncit:C16612 .
  
  lld:C0038525 a ncit:C7057 .
  
  dgn-gda:DGN4a7229b61964fa003bf351171084edc7 sio:SIO_000628 miriam-gene:81618, lld:C0038525;
    a sio:SIO_001122 .
}

dgn-np:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_provenance {
  dgn-np:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_assertion dcterms:description
      "[Genotypes for ERLIN1, TRAPPC9, and WNK2 may prove informative for assessment of the genetic risk for intracerebral hemorrhage, and those for ITM2C and MAPKAP1 may be beneficial in assessment of the genetic risk for subarachnoid hemorrhage in Japanese individuals.]. 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:20198315;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP133444.RAhEbWfcVhL972o1nrvy9g4dXBeq0LqIbSaUFGKbECEHc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:55+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" .
}