@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg> .
@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:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_head {
  this: np:hasAssertion dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_assertion;
    np:hasProvenance dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_provenance;
    np:hasPublicationInfo dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_assertion a np:Assertion .
  
  dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_provenance a np:Provenance .
  
  dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0041341 a ncit:C7057 .
  
  dgn-gda:DGNf3738b8327ab1960057aef9b07c1652a sio:SIO_000628 miriam-gene:7248, lld:C0041341;
    a sio:SIO_001121 .
}

dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_provenance {
  dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_assertion dcterms:description
      "[A proportion of hamartomas from patients with TSC show loss of heterozygosity (LOH) for DNA markers in the region of either the TSC1 gene on chromosome 9q34 or the TSC2 gene on 16p13.3.]. 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:8566961;
    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:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:56+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" .
}