@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk> .
@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:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_head {
  this: np:hasAssertion dgn-np:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_assertion ;
    np:hasProvenance dgn-np:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_provenance ;
    np:hasPublicationInfo dgn-np:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_assertion a np:Assertion .
  dgn-np:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_provenance a np:Provenance .
  dgn-np:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0751571 a ncit:C7057 .
  dgn-gda:DGN3506e043cf4d252da9102b112abdc883 sio:SIO_000628 miriam-gene:7157 , lld:C0751571 ;
    a sio:SIO_001121 .
}
dgn-np:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_provenance {
  dgn-np:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_assertion dcterms:description "[Thirty to sixty percent of human bladder cancer has a mutation in the p53 gene, and the mutational spectrum bears two characteristics: compared with other cancers, the pattern of mutations is more evenly distributed along the p53 gene, and the mutational hotspots occur at both CpG sites, such as codons 175, 248 and 273, and non-CpG sites, such as codons 280 and 285, the latter two being unique mutational hotspots for bladder and other urinary tract cancers.]. 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:12376482 ;
    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:NP370776.RAmlewU_I7zfNDU14j_lV9V338KaubTc8DMkUDnKteunk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:33+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" .
}