@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs> .
@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:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_head {
  this: np:hasAssertion dgn-np:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_assertion;
    np:hasProvenance dgn-np:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_provenance;
    np:hasPublicationInfo dgn-np:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_assertion a np:Assertion .
  
  dgn-np:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_provenance a np:Provenance .
  
  dgn-np:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_assertion {
  miriam-gene:25 a ncit:C16612 .
  
  lld:C0041341 a ncit:C7057 .
  
  dgn-gda:DGNe425326a9d6b911751998e85434a17a0 sio:SIO_000628 miriam-gene:25, lld:C0041341;
    a sio:SIO_001121 .
}

dgn-np:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_provenance {
  dgn-np:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_assertion dcterms:description
      "[The question of genetic heterogeneity in tuberous sclerosis (TSC) was addressed by genetic linkage studies in eight affected families using nine polymorphic markers (EFD126.3, MCT136, ABO, ABL, AK1, and MCOA12 from distal 9q, and PBGD, MCT128.1, and 1CJ52.208M from distal 11q).]. 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:2769723;
    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:NP253714.RAYtz5QuHZHJcrmwKqwWjM2MhlJ2bax63SDq47R1aCVcs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:22+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" .
}