@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY> .
@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:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_head {
  this: np:hasAssertion dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_assertion ;
    np:hasProvenance dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_provenance ;
    np:hasPublicationInfo dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_assertion a np:Assertion .
  dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_provenance a np:Provenance .
  dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0206644 a ncit:C7057 .
  dgn-gda:DGN523cc8ad2daa6f38bdf441c29c74acb6 sio:SIO_000628 miriam-gene:7157 , lld:C0206644 ;
    a sio:SIO_001121 .
}
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_provenance {
  dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_assertion dcterms:description "[However, a similar staining pattern in apparently normal tissue was also observed in 13/48 sections from other individuals with various skin conditions (melanocytic naevi, psoriasis and normal skin adjacent to malignant melanoma and fibrous histiocytomas), suggesting that this pattern of p53 staining may not be unique to individuals with constitutional p53 mutations.]. 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:8479749 ;
    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:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:13+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" .
}