@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk> .
@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:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_head {
  this: np:hasAssertion dgn-np:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion;
    np:hasProvenance dgn-np:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_provenance;
    np:hasPublicationInfo dgn-np:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion a np:Assertion .
  
  dgn-np:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_provenance a np:Provenance .
  
  dgn-np:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion {
  miriam-gene:4854 a ncit:C16612 .
  
  lld:C0751587 a ncit:C7057 .
  
  dgn-gda:DGNc3f4f4103d37d7f1047df60774205cf3 sio:SIO_000628 miriam-gene:4854, lld:C0751587;
    a sio:SIO_001122 .
}

dgn-np:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_provenance {
  dgn-np:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion dcterms:description
      "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. 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:15851739;
    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:NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:27+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" .
}