@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo> .
@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:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_head {
  this: np:hasAssertion dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_assertion;
    np:hasProvenance dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_provenance;
    np:hasPublicationInfo dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_assertion a np:Assertion .
  
  dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_provenance a np:Provenance .
  
  dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN70a37718e27896e529d11cdc553a0066 sio:SIO_000628 miriam-gene:4360, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_provenance {
  dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_assertion dcterms:description
      "[The identification of this MSH2 founder mutation has important implications for the design of mutation-detection strategies for the southern Chinese population. Since there were major emigrations from Hong Kong and Guangdong province during the 19th and 20th centuries, this finding is also significant for Chinese communities worldwide.]. 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:15042510;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}