@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo> .
@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:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_head {
  this: np:hasAssertion dgn-np:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_assertion ;
    np:hasProvenance dgn-np:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_provenance ;
    np:hasPublicationInfo dgn-np:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_assertion a np:Assertion .
  dgn-np:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_provenance a np:Provenance .
  dgn-np:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  lld:C0678222 a ncit:C7057 .
  dgn-gda:DGNef740e2b316d753dd0b3435344d0a89c sio:SIO_000628 miriam-gene:1029 , lld:C0678222 ;
    a sio:SIO_001121 .
}
dgn-np:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_provenance {
  dgn-np:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_assertion dcterms:description "[Alterations in polymorphic markers selected because they had been found to show a high rate of alterations in breast cancer in previous studies (D17S855, D17S654, D16S421, TH2, D10S197, and D9S161), as well as mutations in the p53 gene and aberrant methylation at the first exon of p16INK4a, were used to identify and characterize tumor and plasma DNA.]. 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:10397273 ;
    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:NP174944.RAXwwlNlIXGHFT85RylsvAzWYBSLHh231fV-9OCuioANo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:34+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" .
}