@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw> .
@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/v4.0.0/void/> .

dgn-np:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_head {
  this: np:hasAssertion dgn-np:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_assertion;
    np:hasProvenance dgn-np:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_provenance;
    np:hasPublicationInfo dgn-np:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_assertion a np:Assertion .
  
  dgn-np:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_provenance a np:Provenance .
  
  dgn-np:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0042769 a ncit:C7057 .
  
  dgn-gda:DGNa94ecd03db804aedcd27c6a1367fa4c0 sio:SIO_000628 miriam-gene:348, lld:C0042769;
    a sio:SIO_001121 .
}

dgn-np:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_provenance {
  dgn-np:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_assertion dcterms:description
      "[We investigated if APOE genotype is associated with an increased risk for cerebral palsy, influences the type of cerebral palsy or interacts with prenatal viral infection to influence risk of cerebral palsy.]. 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:18810496;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP694483.RALQtuQ8G-vnFGjN1h7fn60_sOz_pxETvbBtriKDfMVxw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:00+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}