@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI> .
@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:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_head {
  this: np:hasAssertion dgn-np:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_assertion;
    np:hasProvenance dgn-np:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_provenance;
    np:hasPublicationInfo dgn-np:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_assertion a np:Assertion .
  
  dgn-np:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_provenance a np:Provenance .
  
  dgn-np:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGNad851a34208b93475785ec2d2fc8e975 sio:SIO_000628 miriam-gene:7248, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_provenance {
  dgn-np:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_assertion dcterms:description
      "[These data indicate that biallelic inactivation of TSC1 or TSC2 is not frequent in sporadic RCC and suggests that the molecular mechanisms of renal carcinogenesis in TSC are likely to be distinct.]. 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:11710839;
    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:NP266489.RA7Zq3TSuCvnLIzXhNUmaSO44fx9HZkcQdX6t4UUO6lpI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}