@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk> .
@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:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_head {
  this: np:hasAssertion dgn-np:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_assertion;
    np:hasProvenance dgn-np:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_provenance;
    np:hasPublicationInfo dgn-np:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_assertion a np:Assertion .
  
  dgn-np:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_provenance a np:Provenance .
  
  dgn-np:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_assertion {
  miriam-gene:472 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN9730d90a601d8b58079c4911030f8c3b sio:SIO_000628 miriam-gene:472, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_provenance {
  dgn-np:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_assertion dcterms:description
      "[In this study, the functional consequences of specific ATM SNPs on in vitro radiosensitivity, as assessed by micronuclei (MN) formation, were measured in lymphoblastoid cell lines established from 10 breast cancer (BC) patients carrying different ATM missense SNPs, six A-T patients, six A-T heterozygotes (A-T het), and six normal individuals.]. 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:15101044;
    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:NP440974.RAmjisPa1eCNDvOBFI_Ue7WliLKDHn8XD0F7Knpi3I5Hk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:05+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" .
}