@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE> .
@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:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_head {
  this: np:hasAssertion dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_assertion ;
    np:hasProvenance dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_provenance ;
    np:hasPublicationInfo dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_assertion a np:Assertion .
  dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_provenance a np:Provenance .
  dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_assertion {
  miriam-gene:404672 a ncit:C16612 .
  lld:C0043346 a ncit:C7057 .
  dgn-gda:DGN676f276b874354248867e00fb19616ff sio:SIO_000628 miriam-gene:404672 , lld:C0043346 ;
    a sio:SIO_001121 .
}
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_provenance {
  dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_assertion dcterms:description "[However, three further cell strains (TTD4VI and TTD6VI from two French siblings and TTD1BR from an English patient) showed restoration of normal UV-induced DNA repair synthesis after fusion with XP or TTD cells belonging to XP group D. These observations, which give the first indication that TTD is associated with repair defects behaving differently in the functional test of complementation, suggest some kind of causal connection between defective excision-repair factors and clinical features diagnostic for TTD.]. 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:8508495 ;
    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:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:42+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" .
}